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{
"count": 221277,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=230",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=228",
"results": [
{
"created": "2025-05-09T14:38:47.396627+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.707",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs4 has been classified as Green List (High Evidence).",
"entity_name": "NDUFS4",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:38:45.349666+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.707",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS4 were changed from Leigh syndrome, 256000 (3) to Mitochondrial complex I deficiency, nuclear type 1, MIM#252010",
"entity_name": "NDUFS4",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:38:18.403418+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.706",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF5 as ready",
"entity_name": "NDUFAF5",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:38:18.392654+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.706",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf5 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF5",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:38:15.596405+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.706",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF5 were changed from Mitochondrial complex 1 deficiency, 252010 (3) to Mitochondrial complex I deficiency, nuclear type 16 MIM#618238",
"entity_name": "NDUFAF5",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:37:55.679701+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF2 as ready",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:37:55.669602+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf2 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:37:53.310617+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF2 were changed from Leigh syndrome, 256000 (3) to Mitochondrial complex I deficiency, nuclear type 10, MIM#618233",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:37:42.650274+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.704",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFAF2 were set to ",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:37:23.571720+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.703",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDRG1 as ready",
"entity_name": "NDRG1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:37:23.565468+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.703",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndrg1 has been classified as Green List (High Evidence).",
"entity_name": "NDRG1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:37:21.464513+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.703",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDRG1 were changed from Charcot-Marie-Tooth disease, type 4D, 601455 (3) to Charcot-Marie-Tooth disease, type 4D MIM#601455",
"entity_name": "NDRG1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:36:58.742377+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.702",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDP as ready",
"entity_name": "NDP",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:36:58.734983+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.702",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndp has been classified as Green List (High Evidence).",
"entity_name": "NDP",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:36:55.617537+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.702",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDP were changed from Norrie disease, 310600 (3) to Norrie disease, MIM# 310600",
"entity_name": "NDP",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:36:45.224268+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.701",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDP were set to ",
"entity_name": "NDP",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:36:23.449167+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.700",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDE1 as ready",
"entity_name": "NDE1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:36:23.441787+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.700",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nde1 has been classified as Green List (High Evidence).",
"entity_name": "NDE1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:36:20.857165+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.700",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDE1 were changed from Lissencephaly 4 (with microcephaly), 614019 (3) to Lissencephaly 4 (with microcephaly), MIM#614019",
"entity_name": "NDE1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:36:08.095009+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.699",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDE1 were set to ",
"entity_name": "NDE1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:35:47.967346+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.698",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NCF2 as ready",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:35:47.957245+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.698",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ncf2 has been classified as Green List (High Evidence).",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:35:45.496505+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.698",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NCF2 were changed from Chronic granulomatous disease due to deficiency of NCF-2, 233710 (3) to Chronic granulomatous disease 2, autosomal recessive, MIM# 233710",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:35:34.881088+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.697",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NCF2 were set to ",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:34:01.272625+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.696",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NBN as ready",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:34:01.265782+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.696",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nbn has been classified as Green List (High Evidence).",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:33:58.461898+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.696",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NBN were changed from Nijmegen breakage syndrome, 251260 (3) to Nijmegen breakage syndrome (MIM#251260)",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:33:49.281778+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.695",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NBN were set to ",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:33:27.333962+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.694",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NARS2 as ready",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:33:27.324164+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.694",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nars2 has been classified as Green List (High Evidence).",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:33:22.918470+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.694",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NARS2 were changed from Combined oxidative phosphorylation deficiency 24, 616239 (3) to Combined oxidative phosphorylation deficiency 24 - MIM#616239, MONDO:0014547",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:33:12.617529+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.693",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NARS2 were set to ",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:32:01.824599+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.692",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NALCN as ready",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:32:01.817460+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.692",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nalcn has been classified as Green List (High Evidence).",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:31:29.860766+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.692",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NALCN were changed from Hypotonia, infantile, with psychomotor retardation and characteristic facies, 615419 (3) to Hypotonia, infantile, with psychomotor retardation and characteristic facies 1 (MIM#615419)",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:31:17.754625+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.691",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NALCN were set to ",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:30:38.896893+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.690",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NAGS as ready",
"entity_name": "NAGS",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:30:38.889791+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.690",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nags has been classified as Green List (High Evidence).",
"entity_name": "NAGS",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:30:17.312807+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.690",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NAGS were changed from N-acetylglutamate synthase deficiency, 237310 (3) to N-acetylglutamate synthase deficiency MIM#237310",
"entity_name": "NAGS",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:29:55.551190+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.689",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NAGS were set to ",
"entity_name": "NAGS",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:29:36.161468+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.688",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NAGLU as ready",
"entity_name": "NAGLU",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:29:36.151646+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.688",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: naglu has been classified as Green List (High Evidence).",
"entity_name": "NAGLU",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:29:34.029959+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.688",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NAGLU were changed from Mucopolysaccharidosis type IIIB (Sanfilippo B), 252920 (3) to Mucopolysaccharidosis type IIIB (Sanfilippo B) MIM#252920",
"entity_name": "NAGLU",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:29:23.944463+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.687",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NAGLU were set to ",
"entity_name": "NAGLU",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:29:01.437200+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.686",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NAGA as ready",
"entity_name": "NAGA",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:29:01.426331+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.686",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: naga has been classified as Green List (High Evidence).",
"entity_name": "NAGA",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:28:58.832326+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.686",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NAGA were changed from Schindler disease, type I, 609241 (3) to Schindler disease, type I MIM#609241; Schindler disease, type III MIM#609241",
"entity_name": "NAGA",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:28:38.370792+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.685",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NAGA were set to ",
"entity_name": "NAGA",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:27:39.250179+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO7A as ready",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:27:39.240162+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo7a has been classified as Green List (High Evidence).",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:27:34.997888+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO7A were changed from Usher syndrome, type 1B, 276900 (3) to Usher syndrome, type 1B, MIM# 276900",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:27:25.544188+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.683",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO7A were set to ",
"entity_name": "MYO7A",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:27:00.560891+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO5B as ready",
"entity_name": "MYO5B",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:27:00.553714+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo5b has been classified as Green List (High Evidence).",
"entity_name": "MYO5B",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:26:58.261132+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO5B were changed from Microvillus inclusion disease, 251850 (3) to Cholestasis, progressive familial intrahepatic, 10, MIM#619868; Diarrhea 2, with microvillus atrophy, with or without cholestasis, MIM#251850",
"entity_name": "MYO5B",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:26:45.186678+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.681",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO5B were set to ",
"entity_name": "MYO5B",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:26:22.631843+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MVK as ready",
"entity_name": "MVK",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:26:22.621674+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mvk has been classified as Green List (High Evidence).",
"entity_name": "MVK",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:26:20.454312+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MVK were changed from Mevalonic aciduria, 610377 (3) to Mevalonic aciduria, MIM#610377; Hyper-IgD syndrome, MIM#260920",
"entity_name": "MVK",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:26:09.752986+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.679",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MVK were set to ",
"entity_name": "MVK",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:25:46.087913+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.678",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MUT as ready",
"entity_name": "MUT",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:25:46.081503+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.678",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mut has been classified as Green List (High Evidence).",
"entity_name": "MUT",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:25:40.471384+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.678",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MUT were changed from Methylmalonic aciduria, mut(0) type, 251000 (3) to Methylmalonic aciduria, mut(0) type, MIM# 251000",
"entity_name": "MUT",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:25:17.653787+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MUSK as ready",
"entity_name": "MUSK",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:25:17.641094+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: musk has been classified as Green List (High Evidence).",
"entity_name": "MUSK",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:25:15.333979+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MUSK were changed from Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency, 616325 (3) to Fetal akinesia deformation sequence 1 MIM#208150; Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency MIM#616325",
"entity_name": "MUSK",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:25:04.757777+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.676",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MUSK were set to ",
"entity_name": "MUSK",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:24:38.749828+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.675",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MTTP as ready",
"entity_name": "MTTP",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:24:38.743279+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.675",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mttp has been classified as Green List (High Evidence).",
"entity_name": "MTTP",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:24:35.732225+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.675",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MTTP were changed from Abetalipoproteinemia, 200100 (3) to Abetalipoproteinaemia MIM#200100",
"entity_name": "MTTP",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:24:24.728946+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.674",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MTTP were set to ",
"entity_name": "MTTP",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:23:04.153750+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MTRR as ready",
"entity_name": "MTRR",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:23:04.147399+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mtrr has been classified as Green List (High Evidence).",
"entity_name": "MTRR",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:22:31.323440+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MTRR were changed from Homocystinuria-megaloblastic anemia, cbl E type, 236270 (3) to Homocystinuria-megaloblastic anemia, cbl E type, MIM #236270",
"entity_name": "MTRR",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:22:20.674608+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MTRR were set to ",
"entity_name": "MTRR",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:21:54.542611+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MTR as ready",
"entity_name": "MTR",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:21:54.535703+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mtr has been classified as Green List (High Evidence).",
"entity_name": "MTR",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:21:51.184822+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MTR were changed from Homocystinuria-megaloblastic anemia, cblG complementation type, 250940 (3) to Homocystinuria-megaloblastic anaemia, cblG complementation type, MIM# 250940",
"entity_name": "MTR",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:21:39.627451+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MTR were set to ",
"entity_name": "MTR",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:21:18.016796+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MTMR2 as ready",
"entity_name": "MTMR2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:21:18.006353+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mtmr2 has been classified as Green List (High Evidence).",
"entity_name": "MTMR2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:21:15.522844+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MTMR2 were changed from Charcot-Marie-Tooth disease, type 4B1, 601382 (3) to Charcot-Marie-Tooth disease, type 4B1, MIM#601382",
"entity_name": "MTMR2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:20:45.406881+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MTM1 as ready",
"entity_name": "MTM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:20:45.396876+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mtm1 has been classified as Green List (High Evidence).",
"entity_name": "MTM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:20:43.199334+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MTM1 were changed from Myotubular myopathy, X-linked, 310400 (3) to Myopathy, centronuclear, X-linked MIM#310400",
"entity_name": "MTM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:20:33.937807+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MTM1 were set to ",
"entity_name": "MTM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:20:10.859806+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MTHFR as ready",
"entity_name": "MTHFR",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:20:10.850686+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mthfr has been classified as Green List (High Evidence).",
"entity_name": "MTHFR",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:19:57.280528+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MTHFR were changed from Homocystinuria due to MTHFR deficiency, 236250 (3) to Homocystinuria due to MTHFR deficiency, MIM# 236250",
"entity_name": "MTHFR",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:19:47.025019+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.665",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MTHFR were set to ",
"entity_name": "MTHFR",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:59:06.493770+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MTFMT as ready",
"entity_name": "MTFMT",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:59:06.484650+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mtfmt has been classified as Green List (High Evidence).",
"entity_name": "MTFMT",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:59:02.245667+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MTFMT were changed from Combined oxidative phosphorylation deficiency 15, 614947 (3) to Combined oxidative phosphorylation deficiency 15, MIM#614947",
"entity_name": "MTFMT",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:58:52.109333+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.663",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MTFMT were set to ",
"entity_name": "MTFMT",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:58:31.142445+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRE11 as ready",
"entity_name": "MRE11",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:58:31.132613+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mre11 has been classified as Green List (High Evidence).",
"entity_name": "MRE11",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:58:27.252658+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MRE11 were changed from Ataxia-telangiectasia-like disorder, 604391 (3) to Ataxia-telangiectasia-like disorder, MIM#604391",
"entity_name": "MRE11",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:58:15.630601+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.661",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MRE11 were set to ",
"entity_name": "MRE11",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:57:55.885901+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.660",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPV17 as ready",
"entity_name": "MPV17",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:57:55.876232+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.660",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpv17 has been classified as Green List (High Evidence).",
"entity_name": "MPV17",
"entity_type": "gene"
}
]
}