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{
"count": 220489,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1275",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1273",
"results": [
{
"created": "2021-07-07T18:34:30.883251+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.448",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WDR60 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR60",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:33:55.223823+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.447",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WDR60: Rating: GREEN; Mode of pathogenicity: None; Publications: 23910462, 29271569, 26874042; Phenotypes: Short-rib thoracic dysplasia 8 with or without polydactyly, MIM# 615503, Retinitis pigmentosa; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR60",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:30:45.475296+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.447",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR34 as ready",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:30:45.411518+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.447",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr34 has been classified as Green List (High Evidence).",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:27:37.323490+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.447",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR34 were changed from to Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633; Retinitis pigmentosa",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:27:15.838989+10:00",
"panel_name": "Retinitis pigmentosa_Autosomal Recessive/X-linked",
"panel_id": 277,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR34 as ready",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:27:15.816210+10:00",
"panel_name": "Retinitis pigmentosa_Autosomal Recessive/X-linked",
"panel_id": 277,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr34 has been classified as Red List (Low Evidence).",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:27:05.375955+10:00",
"panel_name": "Retinitis pigmentosa_Autosomal Recessive/X-linked",
"panel_id": 277,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WDR34 was added\ngene: WDR34 was added to Retinitis pigmentosa_Autosomal Recessive/X-linked. Sources: Literature\nMode of inheritance for gene: WDR34 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: WDR34 were set to 33124039\nPhenotypes for gene: WDR34 were set to Retinitis pigmentosa\nReview for gene: WDR34 was set to RED\nAdded comment: Single case report of association with RP. Gene-disease association well established for skeletal ciliopathy. \nSources: Literature",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:25:30.434566+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR34 as ready",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:25:30.421802+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr34 has been classified as Green List (High Evidence).",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:25:28.022053+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR34 were changed from to Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:25:02.775001+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WDR34 were set to ",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:24:34.488374+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WDR34 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:24:10.910444+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.95",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WDR34: Rating: GREEN; Mode of pathogenicity: None; Publications: 24183449, 24183451, 30649997, 29241935, 28379358; Phenotypes: Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:23:17.917478+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR34 as ready",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:23:17.905914+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr34 has been classified as Green List (High Evidence).",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:23:10.131608+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR34 were changed from to Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633; Retinitis pigmentosa",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:22:50.643954+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8253",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WDR34 were set to ",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:22:30.637473+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8252",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WDR34 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:22:12.508213+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8251",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WDR34: Rating: GREEN; Mode of pathogenicity: None; Publications: 24183449, 24183451, 33124039, 30649997, 29241935, 28379358; Phenotypes: Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633, Retinitis pigmentosa; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:22:11.744932+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.446",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WDR34 were set to ",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:21:32.927156+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WDR34 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:21:04.256830+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WDR34: Rating: GREEN; Mode of pathogenicity: None; Publications: 24183449, 24183451, 33124039, 30649997, 29241935, 28379358; Phenotypes: Short-rib thoracic dysplasia 11 with or without polydactyly, MIM# 615633, Retinitis pigmentosa; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:04:55.863672+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8251",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR19 as ready",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:04:55.852751+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8251",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr19 has been classified as Green List (High Evidence).",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:04:48.014915+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8251",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR19 were changed from to Nephronophthisis 13, MIM# 614377; Senior-Loken syndrome 8, MIM# 616307; Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376; Cranioectodermal dysplasia 4, MIM# 614378",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:04:30.350255+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WDR19 were set to ",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:04:13.186070+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8249",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WDR19 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:03:54.208461+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8248",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WDR19: Rating: GREEN; Mode of pathogenicity: None; Publications: 33946315, 33875766, 33606107, 22019273, 23559409, 23683095, 32055034; Phenotypes: Nephronophthisis 13, MIM# 614377, Senior-Loken syndrome 8, MIM# 616307, Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376, Cranioectodermal dysplasia 4, MIM# 614378; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:03:04.655371+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR19 as ready",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:03:04.644836+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr19 has been classified as Green List (High Evidence).",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:02:55.242874+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR19 were changed from to Nephronophthisis 13, MIM# 614377; Senior-Loken syndrome 8, MIM# 616307; Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376; Cranioectodermal dysplasia 4, MIM# 614378",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:02:15.343779+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.443",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WDR19 were set to ",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:01:51.846944+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WDR19 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T18:01:17.393857+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WDR19: Rating: GREEN; Mode of pathogenicity: None; Publications: 33946315, 33875766, 33606107, 22019273, 23559409, 23683095, 32055034; Phenotypes: Nephronophthisis 13, MIM# 614377, Senior-Loken syndrome 8, MIM# 616307, Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376, Cranioectodermal dysplasia 4, MIM# 614378; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR19",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:57:17.190486+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TXNDC15 as ready",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:57:17.181331+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: txndc15 has been classified as Green List (High Evidence).",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:57:15.042528+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TXNDC15 were changed from to Meckel-Gruber syndrome",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:56:52.054189+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TXNDC15 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:56:33.315498+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TXNDC15 were set to ",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:56:11.860323+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TXNDC15 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:55:47.477964+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TXNDC15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:55:43.854953+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8248",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TXNDC15 as ready",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:55:43.844319+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8248",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: txndc15 has been classified as Green List (High Evidence).",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:55:27.495606+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8248",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TXNDC15 were changed from to Meckel-Gruber syndrome",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:54:52.225696+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TXNDC15: Rating: GREEN; Mode of pathogenicity: None; Publications: 30851085, 27894351; Phenotypes: Meckel-Gruber syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:54:43.133446+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8247",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TXNDC15 were set to ",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:53:42.258172+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8246",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TXNDC15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:53:25.293511+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TXNDC15: Rating: GREEN; Mode of pathogenicity: None; Publications: 30851085, 27894351; Phenotypes: Meckel-Gruber syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:52:26.841645+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TXNDC15 as ready",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:52:26.829269+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: txndc15 has been classified as Green List (High Evidence).",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:52:15.352657+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TXNDC15 were changed from to Meckel-Gruber syndrome",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:51:47.398584+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.440",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TXNDC15 were set to ",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:51:19.612715+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.439",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TXNDC15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TXNDC15",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:49:54.191661+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3933",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC8 as ready",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:49:54.181531+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3933",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc8 has been classified as Green List (High Evidence).",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:49:49.246154+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3933",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC8 were changed from to Bardet-Biedl syndrome 8, MIM# 615985",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:49:15.749337+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3932",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC8 were set to ",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:48:49.117457+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3931",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TTC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:48:19.364255+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3930",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TTC8: Rating: GREEN; Mode of pathogenicity: None; Publications: 14520415, 19797195; Phenotypes: Bardet-Biedl syndrome 8, MIM# 615985; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:47:45.748621+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC8 as ready",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:47:45.734448+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc8 has been classified as Green List (High Evidence).",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:47:42.828164+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC8 were changed from to Bardet-Biedl syndrome 8, MIM# 615985",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:47:18.703600+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC8 were set to ",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:46:33.195831+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC8 as ready",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:46:33.183619+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc8 has been classified as Green List (High Evidence).",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:46:26.136083+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC8 were changed from to Bardet-Biedl syndrome 8, MIM# 615985",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:45:58.837317+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8244",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC8 were set to ",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:45:40.588095+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8243",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TTC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:45:22.711418+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TTC8: Rating: GREEN; Mode of pathogenicity: None; Publications: 14520415, 19797195; Phenotypes: Bardet-Biedl syndrome 8, MIM# 615985; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:44:28.196583+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC8 as ready",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:44:28.185602+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc8 has been classified as Green List (High Evidence).",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:44:25.944673+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC8 were changed from to Bardet-Biedl syndrome 8, MIM# 615985",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:44:01.807657+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC8 were set to ",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:43:32.325122+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TTC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:42:33.841474+10:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC21B as ready",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:42:33.831803+10:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc21b has been classified as Green List (High Evidence).",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:42:23.111009+10:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC21B were changed from Bardet-Biedl syndrome to Nephronophthisis 12, MIM# 613820; Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:42:12.677153+10:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.249",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC21B were set to ",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:42:02.398054+10:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.248",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TTC21B as Green List (high evidence)",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:42:02.388201+10:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.248",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc21b has been classified as Green List (High Evidence).",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:41:50.569933+10:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.247",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TTC21B: Rating: GREEN; Mode of pathogenicity: None; Publications: 21258341, 25492405, 18327258, 33875766; Phenotypes: Nephronophthisis 12, MIM# 613820, Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:41:04.930655+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.355",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC21B as ready",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:41:04.912253+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.355",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc21b has been classified as Red List (Low Evidence).",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:41:02.147389+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.355",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC21B were changed from to Nephronophthisis 12, MIM# 613820; Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819; Joubert syndrome",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:40:38.073220+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.354",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TTC21B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:40:19.539479+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.353",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TTC21B as Red List (low evidence)",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:40:19.529323+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.353",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc21b has been classified as Red List (Low Evidence).",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:39:55.977174+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.352",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TTC21B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Nephronophthisis 12, MIM# 613820, Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819, Joubert syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:38:44.116643+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC21B as ready",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:38:44.098081+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc21b has been classified as Green List (High Evidence).",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:38:28.809637+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC21B were changed from to Nephronophthisis 12, MIM# 613820; Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819; Joubert syndrome",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:38:05.516601+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8241",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC21B were set to ",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:37:47.480877+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8240",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TTC21B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:37:29.786900+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8239",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TTC21B: Rating: GREEN; Mode of pathogenicity: None; Publications: 21258341, 25492405, 18327258, 33875766; Phenotypes: Nephronophthisis 12, MIM# 613820, Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819, Joubert syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:36:22.621610+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.435",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC21B as ready",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:36:22.612995+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.435",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc21b has been classified as Green List (High Evidence).",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:36:19.437774+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.435",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC21B were changed from to Nephronophthisis 12, MIM# 613820; Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819; Joubert syndrome",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:35:41.338960+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC21B were set to ",
"entity_name": "TTC21B",
"entity_type": "gene"
},
{
"created": "2021-07-07T17:35:15.245497+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TTC21B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TTC21B",
"entity_type": "gene"
}
]
}