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{
"count": 221272,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=222",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=220",
"results": [
{
"created": "2025-05-27T19:39:23.552070+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.977",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rag2 has been classified as Green List (High Evidence).",
"entity_name": "RAG2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:39:19.109829+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.977",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAG2 were changed from Severe combined immunodeficiency, B cell-negative, 601457 (3) to Combined cellular and humoral immune defects with granulomas (MIM#233650); Omenn syndrome (MIM#603554); Severe combined immunodeficiency, B cell-negative (MIM#601457)",
"entity_name": "RAG2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:38:50.562875+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.976",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAG1 as ready",
"entity_name": "RAG1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:38:50.555706+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.976",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rag1 has been classified as Green List (High Evidence).",
"entity_name": "RAG1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:38:46.405791+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.976",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAG1 were changed from Severe combined immunodeficiency, B cell-negative, 601457 (3) to Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity MIM# 609889; Combined cellular and humoral immune defects with granulomas MIM# 233650; Omenn syndrome MIM# 603554; Severe combined immunodeficiency, B cell-negative MIM# 601457",
"entity_name": "RAG1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:38:19.520514+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.975",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAB3GAP2 as ready",
"entity_name": "RAB3GAP2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:38:19.513677+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.975",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rab3gap2 has been classified as Green List (High Evidence).",
"entity_name": "RAB3GAP2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:38:15.366131+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.975",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAB3GAP2 were changed from Warburg micro syndrome 2, 614225 (3) to Warburg micro syndrome MONDO:0016649",
"entity_name": "RAB3GAP2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:38:04.892518+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.974",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RAB3GAP2 were set to ",
"entity_name": "RAB3GAP2",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:37:40.148637+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.973",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAB3GAP1 as ready",
"entity_name": "RAB3GAP1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:37:40.142247+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.973",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rab3gap1 has been classified as Green List (High Evidence).",
"entity_name": "RAB3GAP1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:37:36.011277+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.973",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAB3GAP1 were changed from Warburg micro syndrome 1, 600118 (3) to Warburg micro syndrome 1, MIM# 600118; Martsolf syndrome 2, MIM# 619420",
"entity_name": "RAB3GAP1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:37:25.764766+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RAB3GAP1 were set to ",
"entity_name": "RAB3GAP1",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:37:00.995684+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.971",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAB23 as ready",
"entity_name": "RAB23",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:37:00.988850+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.971",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rab23 has been classified as Green List (High Evidence).",
"entity_name": "RAB23",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:36:56.654810+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.971",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAB23 were changed from Carpenter syndrome, 201000 (3) to Carpenter syndrome MIM#201000",
"entity_name": "RAB23",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:36:46.816057+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RAB23 were set to ",
"entity_name": "RAB23",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:36:23.320414+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAB18 as ready",
"entity_name": "RAB18",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:36:23.314181+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rab18 has been classified as Green List (High Evidence).",
"entity_name": "RAB18",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:36:19.564017+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAB18 were changed from Warburg micro syndrome 3, 614222 (3) to Warburg micro syndrome 3 MIM#614222",
"entity_name": "RAB18",
"entity_type": "gene"
},
{
"created": "2025-05-27T19:36:09.533673+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.968",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RAB18 were set to ",
"entity_name": "RAB18",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:56:39.565605+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.967",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TMEM231 as ready",
"entity_name": "TMEM231",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:56:39.558380+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.967",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: tmem231 has been classified as Green List (High Evidence).",
"entity_name": "TMEM231",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:56:32.252317+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.967",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM231 were changed from Joubert syndrome 20, 614970 (3) to Joubert syndrome 20, MIM#614970; Meckel syndrome 11, MIM#615397",
"entity_name": "TMEM231",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:56:04.682941+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.966",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TMEM231 were set to ",
"entity_name": "TMEM231",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:27:44.966634+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.965",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TMEM237 as ready",
"entity_name": "TMEM237",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:27:44.959299+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.965",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: tmem237 has been classified as Green List (High Evidence).",
"entity_name": "TMEM237",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:27:21.965648+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.965",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM237 were changed from Joubert syndrome 14, 614424 (3) to Joubert syndrome 14, MIM#614424",
"entity_name": "TMEM237",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:27:11.603681+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.964",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TMEM237 were set to ",
"entity_name": "TMEM237",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:26:39.936182+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.963",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TMEM67 as ready",
"entity_name": "TMEM67",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:26:39.927053+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.963",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: tmem67 has been classified as Green List (High Evidence).",
"entity_name": "TMEM67",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:26:35.369785+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.963",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM67 were changed from Joubert syndrome 6, 610688 (3) to COACH syndrome 1 MIM#216360; Joubert syndrome 6 MIM#610688; Meckel syndrome 3 MIM#607361; Nephronophthisis 11 MIM#613550",
"entity_name": "TMEM67",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:26:29.274892+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.962",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TMEM67 were set to ",
"entity_name": "TMEM67",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:26:12.029866+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.961",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TMTC3 as ready",
"entity_name": "TMTC3",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:26:12.023332+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.961",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: tmtc3 has been classified as Green List (High Evidence).",
"entity_name": "TMTC3",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:22:22.644205+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.961",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TMTC3 were changed from Lissencephaly 8, 617255 (3), Autosomal recessive to Lissencephaly 8 MIM#617255, MONDO:0014992",
"entity_name": "TMTC3",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:22:16.775324+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.960",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TMTC3 were set to ",
"entity_name": "TMTC3",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:22:01.544477+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.959",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TOE1 as ready",
"entity_name": "TOE1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:22:01.537272+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.959",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: toe1 has been classified as Green List (High Evidence).",
"entity_name": "TOE1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:21:56.851439+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.959",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TOE1 were changed from Pontocerebellar hypoplasia, type 7, 614969 (3), Autosomal recessive to Pontocerebellar hypoplasia, type 7 MIM#614969",
"entity_name": "TOE1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:21:47.953965+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.958",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TOE1 were set to ",
"entity_name": "TOE1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:18:55.928573+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.957",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TPP1 as ready",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:18:55.921544+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.957",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: tpp1 has been classified as Green List (High Evidence).",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:18:51.844075+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.957",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TPP1 were changed from Ceroid lipofuscinosis, neuronal, 2, 204500 (3) to Ceroid lipofuscinosis, neuronal, 2 MIM#204500; Spinocerebellar ataxia, autosomal recessive 7 MIM#609270",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:18:44.040582+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.956",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TPP1 were set to ",
"entity_name": "TPP1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:18:18.973101+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.955",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TRDN as ready",
"entity_name": "TRDN",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:18:18.966694+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.955",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: trdn has been classified as Green List (High Evidence).",
"entity_name": "TRDN",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:18:15.403590+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.955",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TRDN were changed from Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness, 615441 (3) to Cardiac arrhythmia syndrome, with or without skeletal muscle weakness MIM#615441; Catecholaminergic polymorphic ventricular tachycardia MONDO:0017990",
"entity_name": "TRDN",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:17:54.303898+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.954",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TRDN were set to ",
"entity_name": "TRDN",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:17:40.415989+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.953",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TREX1 as ready",
"entity_name": "TREX1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:17:40.408607+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.953",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: trex1 has been classified as Green List (High Evidence).",
"entity_name": "TREX1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:17:24.875834+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.953",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TREX1 were changed from Aicardi-Goutieres syndrome 1, dominant and recessive, 225750 (3) to Aicardi-Goutieres syndrome 1, dominant and recessive, MIM# 225750, MONDO:0009165",
"entity_name": "TREX1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:17:16.142649+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.952",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TREX1 were set to ",
"entity_name": "TREX1",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:14:40.165173+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.951",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TRIM32 as ready",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:14:40.158727+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.951",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Green List (High Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:14:29.844340+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.951",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TRIM32 were set to 9634523; 10399877; 17994549; 25351777; 19492423, 19303295, 31309175",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:14:16.369918+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.950",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TRIM32 were changed from Muscular dystrophy, limb-girdle, type 2H, 254110 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 8 MIM#254110",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:14:08.486293+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.949",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TRIM32 were set to ",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:08:05.759398+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.948",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TRIM37 as ready",
"entity_name": "TRIM37",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:08:05.752383+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.948",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: trim37 has been classified as Green List (High Evidence).",
"entity_name": "TRIM37",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:08:01.242018+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.948",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TRIM37 were changed from Mulibrey nanism, 253250 (3) to Mulibrey nanism MIM#253250",
"entity_name": "TRIM37",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:07:53.105941+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.947",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TRIM37 were set to ",
"entity_name": "TRIM37",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:07:23.436170+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.946",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TRMU as ready",
"entity_name": "TRMU",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:07:23.428932+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.946",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: trmu has been classified as Green List (High Evidence).",
"entity_name": "TRMU",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:07:19.366895+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.946",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TRMU were changed from Liver failure, transient infantile, 613070 (3) to Liver failure, transient infantile MIM# 613070; acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins MONDO:0013111",
"entity_name": "TRMU",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:07:12.028585+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.945",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TRMU were set to ",
"entity_name": "TRMU",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:06:57.759814+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.944",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TRPM6 as ready",
"entity_name": "TRPM6",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:06:57.753229+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.944",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: trpm6 has been classified as Green List (High Evidence).",
"entity_name": "TRPM6",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:06:53.826862+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.944",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TRPM6 were changed from Hypomagnesemia 1, intestinal, 602014 (3) to Hypomagnesemia 1, intestinal MIM#602014",
"entity_name": "TRPM6",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:06:29.786354+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.943",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TRPM6 were set to ",
"entity_name": "TRPM6",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:05:54.945980+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.942",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TSEN2 as ready",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:05:54.934069+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.942",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: tsen2 has been classified as Green List (High Evidence).",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:05:51.206921+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.942",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TSEN2 were changed from Pontocerebellar hypoplasia type 2B, 612389 (3) to Pontocerebellar hypoplasia type 2B, MIM #612389",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:05:42.865357+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.941",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TSEN2 were set to ",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:03:58.949370+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.940",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TSEN54 as ready",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:03:58.942240+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.940",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: tsen54 has been classified as Green List (High Evidence).",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:03:35.974715+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.940",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TSEN54 were changed from Pontocerebellar hypoplasia type 2A, 277470 (3) to Pontocerebellar hypoplasia type 2A (MIM#277470); Pontocerebellar hypoplasia type 4 (MIM#225753); ?Pontocerebellar hypoplasia type 5 (MIM#610204)",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:03:27.498569+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.939",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TSEN54 were set to ",
"entity_name": "TSEN54",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:03:08.615769+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.938",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TSFM as ready",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:03:08.609326+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.938",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: tsfm has been classified as Green List (High Evidence).",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:02:35.603560+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.938",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TSFM were changed from Combined oxidative phosphorylation deficiency 3, 610505 (3) to Combined oxidative phosphorylation deficiency 3, MIM#610505",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:02:28.822067+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.937",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TSFM were set to ",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:01:53.816926+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.936",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TSHB as ready",
"entity_name": "TSHB",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:01:53.805366+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.936",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: tshb has been classified as Green List (High Evidence).",
"entity_name": "TSHB",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:01:49.498420+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.936",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TSHB were changed from Hypothryoidism, congenital, nongoitrous 4, 275100 (3) to Hypothyroidism, congenital, nongoitrous 4 MIM#275100",
"entity_name": "TSHB",
"entity_type": "gene"
},
{
"created": "2025-05-26T23:01:40.351196+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.935",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TSHB were set to ",
"entity_name": "TSHB",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:55:09.147782+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.934",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TTC37 as ready",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:55:09.138825+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.934",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: ttc37 has been classified as Green List (High Evidence).",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:54:45.888845+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.934",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TTC37 were changed from Trichohepatoenteric syndrome 1, 222470 (3) to Trichohepatoenteric syndrome 1 MIM#222470",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:54:34.517170+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.933",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TTC37 were set to ",
"entity_name": "TTC37",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:54:06.326086+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.932",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TTC7A as ready",
"entity_name": "TTC7A",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:54:06.318704+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.932",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: ttc7a has been classified as Green List (High Evidence).",
"entity_name": "TTC7A",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:54:00.815940+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.932",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TTC7A were set to ",
"entity_name": "TTC7A",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:53:33.075279+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.931",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TTC8 as ready",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:53:33.067591+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.931",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: ttc8 has been classified as Green List (High Evidence).",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:53:25.603113+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.931",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TTC8 were changed from Bardet-Biedl syndrome 8, 615985 (3) to Bardet-Biedl syndrome 8, MIM #615985",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:53:19.307738+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.930",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: TTC8 were set to ",
"entity_name": "TTC8",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:52:21.269522+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.929",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: TTPA as ready",
"entity_name": "TTPA",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:52:21.258951+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.929",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: ttpa has been classified as Green List (High Evidence).",
"entity_name": "TTPA",
"entity_type": "gene"
},
{
"created": "2025-05-26T22:52:16.851270+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.929",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: TTPA were changed from Ataxia with isolated vitamin E deficiency, 277460 (3) to Ataxia with isolated vitamin E deficiency MIM#277460",
"entity_name": "TTPA",
"entity_type": "gene"
}
]
}