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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=245",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=243",
"results": [
{
"created": "2025-04-30T14:32:11.050817+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.246",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTSD were changed from Ceroid lipofuscinosis, neuronal, 10, 610127 (3) to Ceroid lipofuscinosis, neuronal, 10, MIM# 610127",
"entity_name": "CTSD",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:31:42.496104+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTSC as ready",
"entity_name": "CTSC",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:31:42.486215+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctsc has been classified as Green List (High Evidence).",
"entity_name": "CTSC",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:31:40.294599+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTSC were changed from Papillon-Lefevre syndrome, 245000 (3) to Haim-Munk syndrome MIM#245010; Papillon-Lefevre syndrome MIM#245000",
"entity_name": "CTSC",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:31:20.396765+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.244",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTSA as ready",
"entity_name": "CTSA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:31:20.386730+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.244",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctsa has been classified as Green List (High Evidence).",
"entity_name": "CTSA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:30:53.189629+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.244",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTSA were changed from Galactosialidosis, 256540 (3) to Galactosialidosis MIM#256540",
"entity_name": "CTSA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:30:44.851451+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.243",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CTSA were set to ",
"entity_name": "CTSA",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:29:47.748347+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CTNS as ready",
"entity_name": "CTNS",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:29:47.740354+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctns has been classified as Green List (High Evidence).",
"entity_name": "CTNS",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:29:45.296412+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CTNS were changed from Cystinosis, nephropathic, 219800 (3) to Cystinosis, nephropathic MIM#219800",
"entity_name": "CTNS",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:29:34.928885+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.241",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CTNS were set to ",
"entity_name": "CTNS",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:28:59.022994+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.240",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CSPP1 as ready",
"entity_name": "CSPP1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:28:59.015781+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.240",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cspp1 has been classified as Green List (High Evidence).",
"entity_name": "CSPP1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:28:56.766504+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.240",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CSPP1 were changed from Joubert syndrome 21, 615636 (3) to Joubert syndrome 21 MIM#615636; MONDO:0014288",
"entity_name": "CSPP1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:28:48.421621+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.239",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CSPP1 were set to ",
"entity_name": "CSPP1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:28:26.440856+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRTAP as ready",
"entity_name": "CRTAP",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:28:26.433686+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crtap has been classified as Green List (High Evidence).",
"entity_name": "CRTAP",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:28:24.194303+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRTAP were changed from Osteogenesis imperfecta, type VII, 610682 (3) to Osteogenesis imperfecta, type VII MIM#610682",
"entity_name": "CRTAP",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:28:15.953277+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.237",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRTAP were set to ",
"entity_name": "CRTAP",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:27:55.099688+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.236",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRB1 as ready",
"entity_name": "CRB1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:27:55.090302+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.236",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crb1 has been classified as Green List (High Evidence).",
"entity_name": "CRB1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:27:52.845460+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.236",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRB1 were changed from Leber congenital amaurosis 8, 613835 (3) to Leber congenital amaurosis 8, MIM#613835",
"entity_name": "CRB1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:27:41.063586+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRB1 were set to ",
"entity_name": "CRB1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:27:14.179905+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.234",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CPT2 as ready",
"entity_name": "CPT2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:27:14.173497+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.234",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cpt2 has been classified as Green List (High Evidence).",
"entity_name": "CPT2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:27:12.122438+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.234",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CPT2 were changed from CPT II deficiency, lethal neonatal, 608836 (3) to CPT II deficiency, infantile MIM#600649; CPT II deficiency, lethal neonatal MIM#608836",
"entity_name": "CPT2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:26:59.343875+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CPT2 were set to ",
"entity_name": "CPT2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:26:40.514114+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CPT1A as ready",
"entity_name": "CPT1A",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:26:40.506950+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cpt1a has been classified as Green List (High Evidence).",
"entity_name": "CPT1A",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:26:11.996888+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CPT1A were changed from CPT deficiency, hepatic, type IA, 255120 (3) to CPT deficiency, hepatic, type IA, MIM#255120",
"entity_name": "CPT1A",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:26:01.531872+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CPT1A were set to ",
"entity_name": "CPT1A",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:25:42.201687+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.230",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CPS1 as ready",
"entity_name": "CPS1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:25:42.195347+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.230",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cps1 has been classified as Green List (High Evidence).",
"entity_name": "CPS1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:25:39.881727+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.230",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CPS1 were changed from Carbamoylphosphate synthetase I deficiency, 237300 (3) to Carbamoylphosphate synthetase I deficiency MIM#237300",
"entity_name": "CPS1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:25:29.270797+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CPS1 were set to ",
"entity_name": "CPS1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:24:45.632505+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COX15 as ready",
"entity_name": "COX15",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:24:45.624872+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox15 has been classified as Green List (High Evidence).",
"entity_name": "COX15",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:24:43.018044+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX15 were changed from Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2, 615119 (3) to Mitochondrial complex IV deficiency, nuclear type 6, MIM #615119",
"entity_name": "COX15",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:24:32.034059+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.227",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COX15 were set to ",
"entity_name": "COX15",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:24:13.880704+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COLQ as ready",
"entity_name": "COLQ",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:24:13.873862+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: colq has been classified as Green List (High Evidence).",
"entity_name": "COLQ",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:24:07.475498+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COLQ were changed from Myasthenic syndrome, congenital, 5, 603034 (3) to Myasthenic syndrome, congenital, 5 MIM#603034; MONDO:0011281",
"entity_name": "COLQ",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:23:57.397572+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COLQ were set to ",
"entity_name": "COLQ",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:23:39.233732+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COLEC11 as ready",
"entity_name": "COLEC11",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:23:39.226092+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: colec11 has been classified as Green List (High Evidence).",
"entity_name": "COLEC11",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:23:37.003198+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COLEC11 were changed from 3MC syndrome 2, 265050 (3) to 3MC syndrome 2, MIM# 265050; MONDO:0009927",
"entity_name": "COLEC11",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:23:27.591331+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COLEC11 were set to ",
"entity_name": "COLEC11",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:23:10.031360+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL7A1 as ready",
"entity_name": "COL7A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:23:10.024663+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col7a1 has been classified as Green List (High Evidence).",
"entity_name": "COL7A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:23:00.213876+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL7A1 were changed from Epidermolysis bullosa dystrophica, AR, 226600 (3) to Epidermolysis bullosa dystrophica inversa MIM#226600; Epidermolysis bullosa dystrophica, autosomal recessive MIM#226600; Epidermolysis bullosa dystrophica, localisata variant MIM#226600; Epidermolysis bullosa pruriginosa MIM#604129",
"entity_name": "COL7A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:22:29.466889+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COL7A1 were set to ",
"entity_name": "COL7A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:22:10.737784+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.220",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL6A1 as ready",
"entity_name": "COL6A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:22:10.726971+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.220",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col6a1 has been classified as Green List (High Evidence).",
"entity_name": "COL6A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:22:07.749894+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.220",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL6A1 were changed from Ullrich congenital muscular dystrophy 1, 254090 (3) to Ullrich congenital muscular dystrophy 1A MIM#254090",
"entity_name": "COL6A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:21:57.585237+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.219",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COL6A1 were set to ",
"entity_name": "COL6A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:21:15.112689+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.218",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL4A5 as ready",
"entity_name": "COL4A5",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:21:15.104831+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.218",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col4a5 has been classified as Green List (High Evidence).",
"entity_name": "COL4A5",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:21:12.649398+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.218",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL4A5 were changed from Alport syndrome 1, X-linked to Alport syndrome 1, X-linked, MIM#301050",
"entity_name": "COL4A5",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:20:59.074928+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.217",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COL4A5 were set to ",
"entity_name": "COL4A5",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:20:41.338049+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.216",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL4A4 as ready",
"entity_name": "COL4A4",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:20:41.331004+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.216",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col4a4 has been classified as Green List (High Evidence).",
"entity_name": "COL4A4",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:20:36.493409+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.216",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL4A4 were changed from Alport syndrome, autosomal recessive, 203780 (3) to Alport syndrome 2, autosomal recessive MIM# 203780",
"entity_name": "COL4A4",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:20:26.107863+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COL4A4 were set to ",
"entity_name": "COL4A4",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:20:10.555236+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.214",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL4A3 as ready",
"entity_name": "COL4A3",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:20:10.547796+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.214",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col4a3 has been classified as Green List (High Evidence).",
"entity_name": "COL4A3",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:20:08.224293+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.214",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL4A3 were changed from Alport syndrome, autosomal recessive, 203780 (3) to Alport syndrome 3b, autosomal recessive MIM#620536; MONDO:0957811",
"entity_name": "COL4A3",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:19:58.479966+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.213",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COL4A3 were set to ",
"entity_name": "COL4A3",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:19:39.710388+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL27A1 as ready",
"entity_name": "COL27A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:19:39.704203+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col27a1 has been classified as Green List (High Evidence).",
"entity_name": "COL27A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:19:36.725886+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL27A1 were changed from Steel Syndrome to Steel syndrome (MIM#615155)",
"entity_name": "COL27A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:19:26.915300+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.211",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COL27A1 were set to ",
"entity_name": "COL27A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:19:10.609378+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL18A1 as ready",
"entity_name": "COL18A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:19:10.603135+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col18a1 has been classified as Green List (High Evidence).",
"entity_name": "COL18A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:19:08.601111+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL18A1 were changed from Knobloch syndrome, type 1, 267750 (3) to Knobloch syndrome, type 1 MIM#267750",
"entity_name": "COL18A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:18:58.138140+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COL18A1 were set to ",
"entity_name": "COL18A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:18:37.301390+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL17A1 as ready",
"entity_name": "COL17A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:18:37.294678+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col17a1 has been classified as Green List (High Evidence).",
"entity_name": "COL17A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:18:35.504836+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL17A1 were changed from Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3) to Epidermolysis bullosa, junctional 4, intermediate, MIM# 619787",
"entity_name": "COL17A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:18:23.544536+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COL17A1 were set to ",
"entity_name": "COL17A1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:18:05.361472+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.206",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL11A2 as ready",
"entity_name": "COL11A2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:18:05.354486+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.206",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col11a2 has been classified as Green List (High Evidence).",
"entity_name": "COL11A2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:18:02.348712+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.206",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL11A2 were changed from Fibrochondrogenesis 2, 614524 (3) to Deafness, autosomal recessive 53 MIM#609706; Fibrochondrogenesis 2 MIM#614524; Otospondylomegaepiphyseal dysplasia, autosomal recessive MIM#215150",
"entity_name": "COL11A2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:17:49.175019+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.205",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COL11A2 were set to ",
"entity_name": "COL11A2",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:17:28.954150+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.204",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CNGB3 as ready",
"entity_name": "CNGB3",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:17:28.942543+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.204",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cngb3 has been classified as Green List (High Evidence).",
"entity_name": "CNGB3",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:17:26.753593+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.204",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CNGB3 were changed from Macular degeneration, juvenile, 248200 (3) to Achromatopsia 3 MIM#262300",
"entity_name": "CNGB3",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:17:19.237846+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.203",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CNGB3 were set to ",
"entity_name": "CNGB3",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:16:53.329580+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLRN1 as ready",
"entity_name": "CLRN1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:16:53.322725+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clrn1 has been classified as Green List (High Evidence).",
"entity_name": "CLRN1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:16:51.560765+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLRN1 were changed from Usher syndrome, type 3A, 276902 (3) to Usher syndrome, type 3A, MIM#276902",
"entity_name": "CLRN1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:16:42.405757+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.201",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CLRN1 were set to ",
"entity_name": "CLRN1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:16:23.766284+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLPB as ready",
"entity_name": "CLPB",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:16:23.759048+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clpb has been classified as Green List (High Evidence).",
"entity_name": "CLPB",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:16:21.194762+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLPB were changed from 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia, 616271 (3) to 3-methylglutaconic aciduria, type VIIB, autosomal recessive (MIM#616271)",
"entity_name": "CLPB",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:16:08.464705+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.199",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CLPB were set to ",
"entity_name": "CLPB",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:15:54.189389+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLP1 as ready",
"entity_name": "CLP1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:15:54.182378+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clp1 has been classified as Green List (High Evidence).",
"entity_name": "CLP1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:15:52.406573+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLP1 were changed from Pontocerebellar hypoplasia, type 10, 615803 (3) to Pontocerebellar hypoplasia, type 10 MIM#615803",
"entity_name": "CLP1",
"entity_type": "gene"
},
{
"created": "2025-04-30T14:15:42.220535+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CLP1 were set to ",
"entity_name": "CLP1",
"entity_type": "gene"
}
]
}