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{
"count": 221272,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=220",
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"results": [
{
"created": "2025-05-27T21:32:55.608856+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1073",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC52A3 were set to ",
"entity_name": "SLC52A3",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:32:15.180752+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1072",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC52A2 as ready",
"entity_name": "SLC52A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:32:15.173810+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1072",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc52a2 has been classified as Green List (High Evidence).",
"entity_name": "SLC52A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:32:07.493898+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1072",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC52A2 were changed from Brown-Vialetto-Van Laere syndrome 2, 614707 (3) to Brown-Vialetto-Van Laere syndrome 2, MIM# 614707",
"entity_name": "SLC52A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:31:17.497419+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1071",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC52A2 were set to ",
"entity_name": "SLC52A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:30:45.180539+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1070",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC46A1 as ready",
"entity_name": "SLC46A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:30:45.160762+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1070",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc46a1 has been classified as Green List (High Evidence).",
"entity_name": "SLC46A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:30:32.203627+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1070",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC46A1 were changed from Folate malabsorption, hereditary, 229050 (3) to Folate malabsorption, hereditary, MIM# 229050",
"entity_name": "SLC46A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:30:15.240727+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1069",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC46A1 were set to ",
"entity_name": "SLC46A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:29:36.565472+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1068",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC45A2 as ready",
"entity_name": "SLC45A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:29:36.558330+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1068",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc45a2 has been classified as Green List (High Evidence).",
"entity_name": "SLC45A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:28:55.839345+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1068",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC45A2 were changed from Albinism, oculocutaneous, type IV, 606574 (3) to Albinism, oculocutaneous, type IV MIM#606574",
"entity_name": "SLC45A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:28:42.692590+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1067",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC45A2 were set to ",
"entity_name": "SLC45A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:23:25.192289+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1066",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC39A4 as ready",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:23:25.182976+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1066",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc39a4 has been classified as Green List (High Evidence).",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:23:19.364937+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1066",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC39A4 were changed from Acrodermatitis enteropathica, 201100 (3) to Acrodermatitis enteropathica, MIM# 201100",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:23:08.803709+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1065",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC39A4 were set to ",
"entity_name": "SLC39A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:22:33.231734+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1064",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC38A8 as ready",
"entity_name": "SLC38A8",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:22:33.224777+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1064",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc38a8 has been classified as Green List (High Evidence).",
"entity_name": "SLC38A8",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:22:22.559481+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1064",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC38A8 were changed from Foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis, 609218 (3) to Foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis (MIM#609218)",
"entity_name": "SLC38A8",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:22:04.959004+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1063",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC38A8 were set to ",
"entity_name": "SLC38A8",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:21:05.086355+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1062",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC37A4 as ready",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:21:05.078090+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1062",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc37a4 has been classified as Green List (High Evidence).",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:20:57.332381+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1062",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC37A4 were changed from Glycogen storage disease Ib, 232220 (3) to Glycogen storage disease Ib MIM#232220; Glycogen storage disease Ic MIM#232240; Glycogen Storage Disease I MONDO:0002413",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:20:44.151247+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1061",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC37A4 were set to ",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:19:07.940324+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1060",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC35A3 as ready",
"entity_name": "SLC35A3",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:19:07.933840+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1060",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc35a3 has been classified as Green List (High Evidence).",
"entity_name": "SLC35A3",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:18:50.765588+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1060",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC35A3 were changed from Arthrogryposis, mental retardation, and seizures (MIM615553) to Arthrogryposis, impaired intellectual development, and seizures MIM#615553",
"entity_name": "SLC35A3",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:18:00.754295+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1059",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC26A3 as ready",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:18:00.748010+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1059",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc26a3 has been classified as Green List (High Evidence).",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:17:44.698679+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1059",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC26A3 were set to ",
"entity_name": "SLC26A3",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:16:51.505465+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1058",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC26A2 as ready",
"entity_name": "SLC26A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:16:51.499204+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1058",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc26a2 has been classified as Green List (High Evidence).",
"entity_name": "SLC26A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:16:40.608036+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1058",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC26A2 were changed from Achondrogenesis Ib, 600972 (3) to Achondrogenesis Ib MIM#600972; Atelosteogenesis, type II MIM#256050; De la Chapelle dysplasia MIM#256050; Diastrophic dysplasia MIM#222600; Diastrophic dysplasia, broad bone-platyspondylic variant MIM#222600; Epiphyseal dysplasia, multiple, 4 MIM#226900",
"entity_name": "SLC26A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:16:25.122169+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1057",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC26A2 were set to ",
"entity_name": "SLC26A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:15:55.531910+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1056",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A15 as ready",
"entity_name": "SLC25A15",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:15:55.516257+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1056",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a15 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A15",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:15:50.474496+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1056",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A15 were changed from Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, 238970 (3) to Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome MIM#238970",
"entity_name": "SLC25A15",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:15:36.068819+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1055",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A15 were set to ",
"entity_name": "SLC25A15",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:14:17.429293+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1054",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A13 as ready",
"entity_name": "SLC25A13",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:14:17.420359+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1054",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a13 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A13",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:14:00.291641+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1054",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A13 were changed from Citrullinemia, type II, neonatal-onset, 605814 (3) to Citrullinemia, type II, neonatal-onset, MIM#605814",
"entity_name": "SLC25A13",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:13:36.984527+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1053",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A13 were set to ",
"entity_name": "SLC25A13",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:13:12.970901+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1052",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A1 as ready",
"entity_name": "SLC25A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:13:12.963546+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1052",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a1 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:13:08.674494+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1052",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A1 were changed from Combined D-2- and L-2-hydroxyglutaric aciduria, 615182 (3) to Combined D-2- and L-2-hydroxyglutaric aciduria, MIM#615182; Myasthenic syndrome, congenital, 23, presynaptic, MIM#618197",
"entity_name": "SLC25A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:12:44.431533+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1051",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A1 were set to ",
"entity_name": "SLC25A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:12:19.715254+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1050",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC22A5 as ready",
"entity_name": "SLC22A5",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:12:19.708444+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1050",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc22a5 has been classified as Green List (High Evidence).",
"entity_name": "SLC22A5",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:12:15.458643+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1050",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC22A5 were changed from Carnitine deficiency, systemic primary, 212140 (3) to Carnitine deficiency, systemic primary, MIM# 212140, MONDO:0008919",
"entity_name": "SLC22A5",
"entity_type": "gene"
},
{
"created": "2025-05-27T21:12:04.440980+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC22A5 were set to ",
"entity_name": "SLC22A5",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:28:16.844613+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC1A4 as ready",
"entity_name": "SLC1A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:28:16.835216+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc1a4 has been classified as Green List (High Evidence).",
"entity_name": "SLC1A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:28:11.039427+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC1A4 were changed from Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, 616657 (3) to Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, MIM# 616657",
"entity_name": "SLC1A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:27:58.185790+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC1A4 were set to ",
"entity_name": "SLC1A4",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:27:31.341495+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1046",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC19A3 as ready",
"entity_name": "SLC19A3",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:27:31.331696+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1046",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc19a3 has been classified as Green List (High Evidence).",
"entity_name": "SLC19A3",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:27:27.148962+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1046",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC19A3 were changed from Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), 607483 (3) to Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), MIM# 607483",
"entity_name": "SLC19A3",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:27:14.815211+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC19A3 were set to ",
"entity_name": "SLC19A3",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:26:36.758489+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC19A2 as ready",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:26:36.749896+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc19a2 has been classified as Green List (High Evidence).",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:26:33.107533+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC19A2 were changed from Thiamine-responsive megaloblastic anemia syndrome, 249270 (3) to Thiamine-responsive megaloblastic anemia syndrome, MIM#249270",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:26:22.114646+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1043",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC19A2 were set to ",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:25:31.212605+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC17A5 as ready",
"entity_name": "SLC17A5",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:25:31.204511+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc17a5 has been classified as Green List (High Evidence).",
"entity_name": "SLC17A5",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:25:27.307816+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC17A5 were changed from Sialic acid storage disorder, infantile, 269920 (3) to Sialic acid storage disorder, infantile (MIM#269920)",
"entity_name": "SLC17A5",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:25:16.516126+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1041",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC17A5 were set to ",
"entity_name": "SLC17A5",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:24:52.598720+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1040",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC16A2 as ready",
"entity_name": "SLC16A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:24:52.590917+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1040",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc16a2 has been classified as Green List (High Evidence).",
"entity_name": "SLC16A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:24:48.686831+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1040",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC16A2 were changed from Allan-Herndon-Dudley syndrome to Allan-Herndon-Dudley syndrome, MIM #300523",
"entity_name": "SLC16A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:24:37.295883+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1039",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC16A2 were set to ",
"entity_name": "SLC16A2",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:24:13.732031+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC12A1 as ready",
"entity_name": "SLC12A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:24:13.722492+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc12a1 has been classified as Green List (High Evidence).",
"entity_name": "SLC12A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:24:09.729993+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC12A1 were changed from Bartter syndrome, type 1, 601678 (3) to Bartter syndrome, type 1, MIM#601678",
"entity_name": "SLC12A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:23:55.728310+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1037",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC12A1 were set to ",
"entity_name": "SLC12A1",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:23:33.100031+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SKIV2L as ready",
"entity_name": "SKIV2L",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:23:33.093524+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: skiv2l has been classified as Green List (High Evidence).",
"entity_name": "SKIV2L",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:23:24.934906+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SKIV2L were changed from Trichohepatoenteric syndrome 2, 614602 (3) to Trichohepatoenteric syndrome 2, MIM# 614602",
"entity_name": "SKIV2L",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:23:13.524529+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1035",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SKIV2L were set to ",
"entity_name": "SKIV2L",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:16:26.903342+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SH3TC2 as ready",
"entity_name": "SH3TC2",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:16:26.896745+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sh3tc2 has been classified as Green List (High Evidence).",
"entity_name": "SH3TC2",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:16:16.913843+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SH3TC2 were changed from Charcot-Marie-Tooth disease, type 4C, 601596 (3) to Charcot-Marie-Tooth disease, type 4C MIM#601596",
"entity_name": "SH3TC2",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:15:36.244575+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SGSH as ready",
"entity_name": "SGSH",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:15:36.235028+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sgsh has been classified as Green List (High Evidence).",
"entity_name": "SGSH",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:15:22.107260+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SGSH were changed from Mucopolysaccharidisis type IIIA (Sanfilippo A), 252900 (3) to Mucopolysaccharidosis type IIIA (Sanfilippo A), MIM# 252900; MONDO:0009655",
"entity_name": "SGSH",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:15:11.564296+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SGSH were set to ",
"entity_name": "SGSH",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:14:45.745370+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SGCG as ready",
"entity_name": "SGCG",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:14:45.735886+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sgcg has been classified as Green List (High Evidence).",
"entity_name": "SGCG",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:14:41.340865+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SGCG were changed from Muscular dystrophy, limb-girdle, type 2C, 253700 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 5 MIM#253700",
"entity_name": "SGCG",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:14:12.283063+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1030",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SGCD as ready",
"entity_name": "SGCD",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:14:12.274316+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1030",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sgcd has been classified as Green List (High Evidence).",
"entity_name": "SGCD",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:14:06.210960+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1030",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SGCD were changed from Muscular dystrophy, limb-girdle, type 2F, 601287 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 6, MIM# 601287",
"entity_name": "SGCD",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:13:49.461553+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1029",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SGCD were set to ",
"entity_name": "SGCD",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:13:24.053021+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1028",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SGCB as ready",
"entity_name": "SGCB",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:13:24.045245+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1028",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sgcb has been classified as Green List (High Evidence).",
"entity_name": "SGCB",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:13:19.456451+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1028",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SGCB were changed from Muscular dystrophy, limb-girdle, type 2E, 604286 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 4 MIM#604286",
"entity_name": "SGCB",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:12:53.229108+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SGCA as ready",
"entity_name": "SGCA",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:12:53.221904+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sgca has been classified as Green List (High Evidence).",
"entity_name": "SGCA",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:12:49.081167+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SGCA were changed from Muscular dystrophy, limb-girdle, type 2D, 608099 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 3 MIM#608099; autosomal recessive limb-girdle muscular dystrophy type 2D, MONDO:0011968",
"entity_name": "SGCA",
"entity_type": "gene"
},
{
"created": "2025-05-27T20:05:24.655494+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.1026",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SGCA were set to ",
"entity_name": "SGCA",
"entity_type": "gene"
}
]
}