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{
"count": 220725,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2007",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2005",
"results": [
{
"created": "2020-01-03T21:05:36.706575+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.601",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: glis2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T21:05:32.020473+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GLIS2 were set to ",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T21:05:15.223604+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.600",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GLIS2: Rating: AMBER; Mode of pathogenicity: None; Publications: 17618285, 23559409; Phenotypes: Nephronophthisis 7, OMIM#611498; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T21:04:55.383003+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GLIS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T21:04:23.944514+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GLIS2 as Amber List (moderate evidence)",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T21:04:23.928207+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: glis2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T21:03:49.207817+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GLIS2: Rating: AMBER; Mode of pathogenicity: None; Publications: 17618285, 23559409; Phenotypes: Nephronophthisis 7, OMIM#611498; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T21:00:34.229105+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.600",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT57 as ready",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-03T21:00:34.217580+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.600",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift57 has been classified as Red List (Low Evidence).",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-03T21:00:05.549234+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.600",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT57 were changed from to Orofaciodigital syndrome XVIII, MIM# 617927",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:59:48.349227+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.599",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT57 were set to ",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:59:31.563291+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.598",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFT57 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:58:46.602691+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.597",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT57 as Red List (low evidence)",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:58:46.590682+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.597",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift57 has been classified as Red List (Low Evidence).",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:58:28.290313+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.596",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IFT57: Rating: RED; Mode of pathogenicity: None; Publications: 27060890; Phenotypes: Orofaciodigital syndrome XVIII, MIM# 617927; Mode of inheritance: None",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:56:09.393326+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.596",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT74 as ready",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:56:09.382400+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.596",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift74 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:55:58.528241+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT74 as ready",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:55:58.514708+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift74 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:55:56.665986+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.596",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT74 as Amber List (moderate evidence)",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:55:56.652773+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.596",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift74 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:55:37.433541+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.595",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IFT74 was added\ngene: IFT74 was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: IFT74 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: IFT74 were set to 27486776\nPhenotypes for gene: IFT74 were set to Bardet-Biedl syndrome 20, MIM# 617119\nReview for gene: IFT74 was set to AMBER\nAdded comment: Single family and functional data. \nSources: Expert list",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:55:26.592076+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT74 as Amber List (moderate evidence)",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:55:26.581216+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift74 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:54:22.748337+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT74 as Amber List (moderate evidence)",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:54:22.735246+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift74 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:53:21.475092+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: IFT74 was added\ngene: IFT74 was added to Bardet Biedl syndrome_VCGS. Sources: Expert list\nMode of inheritance for gene: IFT74 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: IFT74 were set to 27486776\nPhenotypes for gene: IFT74 were set to Bardet-Biedl syndrome 20, MIM# 617119\nReview for gene: IFT74 was set to AMBER\nAdded comment: Single family plus functional data. \nSources: Expert list",
"entity_name": "IFT74",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:49:21.218416+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.594",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT81 as ready",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:49:21.213197+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.594",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Three families with skeletal dysplasia, one with nephronophthisis, one with eye phenotype.",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:49:21.182866+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.594",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Green List (High Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:49:11.106934+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Amber List (moderate evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:49:11.095944+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:48:42.134446+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Amber List (moderate evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:48:42.121475+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:47:48.138929+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to 27666822; 30080953; 28460050; 26275418",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:47:22.895350+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to 27666822; 30080953; 28460050; 26275418",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:46:57.427391+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to 27666822",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:46:49.508182+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.594",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT81 were changed from to Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:45:49.268153+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Green List (high evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:45:49.257077+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Green List (High Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:45:11.564279+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.593",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to 27666822",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:44:36.496264+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to 27666822; 30080953",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:44:17.418673+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Green List (high evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:44:17.398305+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Green List (High Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:43:55.831018+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to 27666822",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:43:29.403127+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Green List (high evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:43:28.997318+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Green List (High Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:43:00.387558+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to 27666822",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:42:21.600522+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Green List (high evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:42:21.587047+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Green List (High Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:41:33.493601+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT81 as ready",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:41:33.487624+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Single family with renal phenotype.",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:41:33.440708+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Red List (Low Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:41:23.532240+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.67",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFT81 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:41:09.194565+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.592",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFT81 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:39:08.995770+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.66",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to ",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:39:03.249253+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT81 were changed from to Short-rib thoracic dysplasia 19 with or without polydactyly; OMIM #617895",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:37:47.328666+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.591",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Green List (high evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:37:47.314669+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.591",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Green List (High Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:37:41.389806+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to 27666822; 26275418",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:36:55.742153+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on publications: Third report identified.",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:36:55.712618+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to 27666822",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:36:30.135361+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Green List (high evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:36:30.015872+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Green List (High Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:34:25.370224+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Amber List (moderate evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:34:25.353639+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:34:08.058303+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.590",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to ",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:33:53.659356+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.589",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Amber List (moderate evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:33:53.644524+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.589",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:33:33.891597+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IFT81: Rating: AMBER; Mode of pathogenicity: None; Publications: 27666822; Phenotypes: Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:33:24.121300+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IFT81: Rating: AMBER; Mode of pathogenicity: None; Publications: 27666822; Phenotypes: Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:31:49.417353+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT81 as ready",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:31:49.404248+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:31:36.214797+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT81 as ready",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:31:36.202417+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:29:58.749750+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT81 as ready",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:29:58.736980+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:29:54.791234+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Amber List (moderate evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:29:54.775573+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:29:52.638503+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFT81 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:29:51.169565+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to ",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:28:44.429968+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFT81 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:28:39.983256+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Amber List (moderate evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:28:39.959504+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:27:50.259344+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to ",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:27:31.335744+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFT81 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:27:12.365829+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT81 were changed from to Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:27:07.009485+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT81 were changed from to Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:27:00.883514+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT81 were changed from to Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:26:21.851086+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFT81 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:26:06.144503+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.31",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFT81 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:25:59.781102+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT81 were set to ",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:25:35.831795+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Amber List (moderate evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:25:35.811336+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:24:57.437229+11:00",
"panel_name": "Short Rib Polydactyly, Jeune Asphyxiating Thoracic Dystrophy_VCGS",
"panel_id": 179,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IFT81: Rating: AMBER; Mode of pathogenicity: None; Publications: 27666822; Phenotypes: Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:24:05.382642+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.30",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IFT81: Rating: AMBER; Mode of pathogenicity: None; Publications: 27666822; Phenotypes: Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:23:27.921434+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IFT81 as Amber List (moderate evidence)",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:23:27.908589+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift81 has been classified as Amber List (Moderate Evidence).",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:22:51.646096+11:00",
"panel_name": "Skeletal dysplasia Fetal_MelbourneGenomics_VCGS",
"panel_id": 28,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IFT81: Rating: AMBER; Mode of pathogenicity: None; Publications: 27666822; Phenotypes: Short-rib thoracic dysplasia 19 with or without polydactyly, MIM# 617895; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT81",
"entity_type": "gene"
},
{
"created": "2020-01-03T20:14:52.241835+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on publications: Second family identified.",
"entity_name": "PDE6D",
"entity_type": "gene"
}
]
}