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{
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"results": [
{
"created": "2021-07-04T15:28:04.188885+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: iqcb1 has been classified as Green List (High Evidence).",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:27:56.819697+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IQCB1 were changed from to Senior-Loken syndrome 5, MIM# 609254; MONDO:0012225",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:27:33.044244+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IQCB1 were set to ",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:27:09.371390+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IQCB1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:26:38.918768+10:00",
"panel_name": "Renal Ciliopathies and Nephronophthisis",
"panel_id": 193,
"panel_version": "0.178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IQCB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 15723066, 21220633, 20881296, 21901789, 33512896, 33535056, 29219953; Phenotypes: Senior-Loken syndrome 5, MIM# 609254, MONDO:0012225; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:25:48.674295+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IQCB1 as ready",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:25:48.665004+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: iqcb1 has been classified as Green List (High Evidence).",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:25:40.375989+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IQCB1 were changed from to Senior-Loken syndrome 5, MIM# 609254; MONDO:0012225",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:25:23.310906+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IQCB1 were set to ",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:25:05.914014+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IQCB1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:24:39.348610+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IQCB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 15723066, 21220633, 20881296, 21901789, 33512896, 33535056, 29219953; Phenotypes: Senior-Loken syndrome 5, MIM# 609254, MONDO:0012225; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:24:22.054698+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.395",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IQCB1 were changed from Senior-Loken syndrome 5, MIM# 609254 to Senior-Loken syndrome 5, MIM# 609254; MONDO:0012225",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:23:30.232107+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.394",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IQCB1 as ready",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:23:30.221637+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.394",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: iqcb1 has been classified as Green List (High Evidence).",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:23:27.858217+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.394",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IQCB1 were changed from to Senior-Loken syndrome 5, MIM# 609254",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:23:04.148380+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.393",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IQCB1 were set to ",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:22:46.899318+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.392",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IQCB1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:21:58.017509+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IQCB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 15723066, 21220633, 20881296, 21901789, 33512896, 33535056, 29219953; Phenotypes: Senior-Loken syndrome 5, MIM# 609254; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IQCB1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:18:36.239164+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HNF1B as ready",
"entity_name": "HNF1B",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:18:36.229349+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hnf1b has been classified as Green List (High Evidence).",
"entity_name": "HNF1B",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:18:32.218657+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.391",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HNF1B were changed from to Renal cysts and diabetes syndrome, MIM# 137920",
"entity_name": "HNF1B",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:18:03.568376+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.390",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: HNF1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "HNF1B",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:17:39.590274+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: HNF1B.",
"entity_name": "HNF1B",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:17:30.863542+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HNF1B: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Renal cysts and diabetes syndrome, MIM# 137920; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "HNF1B",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:16:20.843980+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT80 as ready",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:16:20.828840+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift80 has been classified as Green List (High Evidence).",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:16:18.573691+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT80 were changed from to Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263; MONDO:0012644",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:15:56.472316+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT80 were set to ",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:15:32.397542+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFT80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:15:06.700050+10:00",
"panel_name": "Short Rib Polydactyly_Jeune Asphyxiating Thoracic Dystrophy_Skeletal Ciliopathy",
"panel_id": 179,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IFT80: Rating: GREEN; Mode of pathogenicity: None; Publications: 17468754, 19648123, 30767363; Phenotypes: Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263, MONDO:0012644; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:14:08.175129+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT80 as ready",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:14:08.163833+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift80 has been classified as Green List (High Evidence).",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:14:00.823106+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT80 were changed from to Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263; MONDO:0012644",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:13:42.526244+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT80 were set to ",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:13:22.861320+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFT80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:13:04.970948+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "commented on gene: IFT80: 5 unrelated families reported.",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:12:58.390949+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IFT80: Rating: GREEN; Mode of pathogenicity: None; Publications: 17468754, 19648123, 30767363; Phenotypes: Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263, MONDO:0012644; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:12:33.551254+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT80 were changed from Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263 to Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263; MONDO:0012644",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:11:22.830708+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.388",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT80 as ready",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:11:22.818438+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.388",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift80 has been classified as Green List (High Evidence).",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:11:12.631165+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.388",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT80 were changed from to Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:10:48.128680+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.387",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFT80 were set to ",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:10:20.447294+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.386",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFT80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:09:56.453749+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.385",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IFT80: Rating: GREEN; Mode of pathogenicity: None; Publications: 17468754, 19648123, 30767363; Phenotypes: Short-rib thoracic dysplasia 2 with or without polydactyly, MIM# 611263; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IFT80",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:00:04.414617+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LZTFL1 as ready",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2021-07-04T15:00:04.400689+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lztfl1 has been classified as Green List (High Evidence).",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:59:57.334637+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LZTFL1 were changed from to Bardet-Biedl syndrome 17 (MIM#615994)",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:59:39.111783+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LZTFL1 were set to ",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:59:05.256004+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LZTFL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:54:34.594780+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LZTFL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22510444, 23692385, 27312011, 22072986; Phenotypes: Bardet-Biedl syndrome 17 (MIM#615994); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:53:27.921815+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.385",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LZTFL1 as ready",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:53:27.911416+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.385",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lztfl1 has been classified as Green List (High Evidence).",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:53:25.528101+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.385",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LZTFL1 were changed from to Bardet-Biedl syndrome 17 (MIM#615994)",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:52:58.973934+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.384",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LZTFL1 were set to ",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:52:35.515043+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.383",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LZTFL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:50:42.950040+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.382",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LBR as ready",
"entity_name": "LBR",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:50:42.937208+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.382",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lbr has been classified as Green List (High Evidence).",
"entity_name": "LBR",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:50:40.622288+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.382",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LBR were changed from to Greenberg skeletal dysplasia, MIM#215140",
"entity_name": "LBR",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:50:16.056098+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.381",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LBR were set to ",
"entity_name": "LBR",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:49:56.477808+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.380",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LBR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LBR",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:47:23.747097+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Seven families and functional data including zebrafish model. \r\nSources: Literature; to: Nine families and functional data including zebrafish model. \r\nSources: Literature",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:47:10.643222+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Three unrelated families and functional data including zebrafish model. \nSources: Literature; to: Seven families and functional data including zebrafish model. \r\nSources: Literature",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:46:48.389440+10:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Three unrelated families and functional data including zebrafish model. Cholestasis prominent. \nSources: Literature; to: 7 families and functional data including zebrafish model. Cholestasis prominent. \r\nSources: Literature",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:46:37.827953+10:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC26 as ready",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:46:37.818390+10:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc26 has been classified as Green List (High Evidence).",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:46:26.063550+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Three unrelated families and functional data including zebrafish model. \nSources: Literature; to: 9 families and functional data including zebrafish model. \r\nSources: Literature",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:44:56.101466+10:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TTC26 as Green List (high evidence)",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:44:56.092364+10:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc26 has been classified as Green List (High Evidence).",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:44:24.300854+10:00",
"panel_name": "Cholestasis",
"panel_id": 78,
"panel_version": "0.196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TTC26 was added\ngene: TTC26 was added to Cholestasis. Sources: Literature\nMode of inheritance for gene: TTC26 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TTC26 were set to 34177428; 32617964; 31595528; 24596149; 22718903\nPhenotypes for gene: TTC26 were set to Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations\nReview for gene: TTC26 was set to GREEN\nAdded comment: Three unrelated families and functional data including zebrafish model. Cholestasis prominent. \nSources: Literature",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:43:04.754704+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC26 as ready",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:43:04.741943+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc26 has been classified as Green List (High Evidence).",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:42:56.205108+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TTC26 as Green List (high evidence)",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:42:56.195342+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc26 has been classified as Green List (High Evidence).",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:42:23.738061+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.8185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TTC26 was added\ngene: TTC26 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: TTC26 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TTC26 were set to 34177428; 32617964; 31595528; 24596149; 22718903\nPhenotypes for gene: TTC26 were set to Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations\nReview for gene: TTC26 was set to GREEN\nAdded comment: Three unrelated families and functional data including zebrafish model. \nSources: Literature",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:40:43.360012+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC26 as ready",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:40:43.349887+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc26 has been classified as Green List (High Evidence).",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:40:37.880010+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TTC26 as Green List (high evidence)",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:40:37.870659+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc26 has been classified as Green List (High Evidence).",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:39:25.535777+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.378",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TTC26 was added\ngene: TTC26 was added to Ciliopathies. Sources: Literature\nMode of inheritance for gene: TTC26 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TTC26 were set to 34177428; 32617964; 31595528; 24596149; 22718903\nPhenotypes for gene: TTC26 were set to Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations\nReview for gene: TTC26 was set to GREEN\nAdded comment: Three unrelated families and functional data including zebrafish model. \nSources: Literature",
"entity_name": "TTC26",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:34:16.051207+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.377",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF7 as ready",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:34:16.008657+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.377",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif7 has been classified as Green List (High Evidence).",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:34:12.916994+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.377",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF7 were changed from to Joubert syndrome 12, MIM# 200990; Acrocallosal syndrome, MIM# 200990; MONDO:0008708; Hydrolethalus syndrome 2, MIM# 614120",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:33:38.634072+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.376",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF7 were set to ",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:33:16.722538+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.375",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:32:04.840370+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.374",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIAA0753 as ready",
"entity_name": "KIAA0753",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:32:04.828496+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.374",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kiaa0753 has been classified as Green List (High Evidence).",
"entity_name": "KIAA0753",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:32:01.690075+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.374",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIAA0753 were changed from to Orofaciodigital syndrome XV 617127; Joubert syndrome",
"entity_name": "KIAA0753",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:31:36.998270+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.373",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIAA0753 were set to ",
"entity_name": "KIAA0753",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:31:07.754396+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIAA0753 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KIAA0753",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:30:40.223785+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "KIAA0753",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:29:51.881583+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIAA0586 as ready",
"entity_name": "KIAA0586",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:29:51.871914+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kiaa0586 has been classified as Green List (High Evidence).",
"entity_name": "KIAA0586",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:29:49.180712+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIAA0586 were changed from to Joubert syndrome 23 616490; Short-rib thoracic dysplasia 14 with polydactyly 616546",
"entity_name": "KIAA0586",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:29:19.885170+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.370",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIAA0586 were set to ",
"entity_name": "KIAA0586",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:28:50.031604+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.369",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: KIAA0586: Changed rating: GREEN; Changed publications: 26166481; Changed phenotypes: Short-rib thoracic dysplasia 14 with polydactyly, MIM# 616546; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KIAA0586",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:27:38.231214+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.369",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIAA0586 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KIAA0586",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:27:16.367493+10:00",
"panel_name": "Ciliopathies",
"panel_id": 84,
"panel_version": "0.368",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: KIAA0586.",
"entity_name": "KIAA0586",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:23:59.875537+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT52 as ready",
"entity_name": "IFT52",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:23:59.861944+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift52 has been classified as Green List (High Evidence).",
"entity_name": "IFT52",
"entity_type": "gene"
},
{
"created": "2021-07-04T14:23:57.364373+10:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT52 were changed from to Short-rib thoracic dysplasia 16 with or without polydactyly, MIM# 617102",
"entity_name": "IFT52",
"entity_type": "gene"
}
]
}