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{
"count": 217334,
"next": "https://panelapp.genomicsengland.co.uk/api/v1/activities/?format=api&page=2147",
"previous": "https://panelapp.genomicsengland.co.uk/api/v1/activities/?format=api&page=2145",
"results": [
{
"created": "2016-11-03T19:04:08.348000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on SIGMAR1",
"entity_name": "SIGMAR1",
"entity_type": "gene"
},
{
"created": "2016-11-03T19:04:08.348000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified SIGMAR1 as amber",
"entity_name": "SIGMAR1",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:59:53.652000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PFN1 as amber",
"entity_name": "PFN1",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:59:53.651000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on PFN1",
"entity_name": "PFN1",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:57:22.700000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified HNRNPA1 as amber",
"entity_name": "HNRNPA1",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:57:22.699000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on HNRNPA1",
"entity_name": "HNRNPA1",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:55:31.872000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified ERBB4 as amber",
"entity_name": "ERBB4",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:55:31.871000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on ERBB4",
"entity_name": "ERBB4",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:53:00.670000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified CHCHD10 as red",
"entity_name": "CHCHD10",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:53:00.669000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on CHCHD10",
"entity_name": "CHCHD10",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:51:15.536000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked ATXN2 as ready",
"entity_name": "ATXN2",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:51:04.114000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified ATXN2 as red",
"entity_name": "ATXN2",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:46:58.733000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified SLC52A3 as amber",
"entity_name": "SLC52A3",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:41:32.191000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on SLC52A2",
"entity_name": "SLC52A2",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:40:51.486000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified SLC52A2 as amber",
"entity_name": "SLC52A2",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:36:32.519000Z",
"panel_name": "Amyotrophic lateral sclerosis/motor neuron disease",
"panel_id": 263,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified SLC52A1 as amber",
"entity_name": "SLC52A1",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:18:14.350000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified VPS13A as amber",
"entity_name": "VPS13A",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:18:14.349000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on VPS13A",
"entity_name": "VPS13A",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:14:15.621000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified UCHL1 as red",
"entity_name": "UCHL1",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:14:15.620000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on UCHL1",
"entity_name": "UCHL1",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:12:23.988000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked TBP as ready",
"entity_name": "TBP",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:12:12.316000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified TBP as red",
"entity_name": "TBP",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:09:04.225000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified SYNJ1 as amber",
"entity_name": "SYNJ1",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:09:04.224000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on SYNJ1",
"entity_name": "SYNJ1",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:02:09.170000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified SPG11 as amber",
"entity_name": "SPG11",
"entity_type": "gene"
},
{
"created": "2016-11-03T18:02:09.169000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on SPG11",
"entity_name": "SPG11",
"entity_type": "gene"
},
{
"created": "2016-11-03T17:55:19.298000Z",
"panel_name": "Hyperammonaemia",
"panel_id": 267,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on ETFDH",
"entity_name": "ETFDH",
"entity_type": "gene"
},
{
"created": "2016-11-03T17:51:56.691000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified SNCAIP as red",
"entity_name": "SNCAIP",
"entity_type": "gene"
},
{
"created": "2016-11-03T17:51:56.689000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on SNCAIP",
"entity_name": "SNCAIP",
"entity_type": "gene"
},
{
"created": "2016-11-03T17:49:51.353000Z",
"panel_name": "Hyperammonaemia",
"panel_id": 267,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on ETFB",
"entity_name": "ETFB",
"entity_type": "gene"
},
{
"created": "2016-11-03T17:45:32.804000Z",
"panel_name": "Hyperammonaemia",
"panel_id": 267,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on ETFA",
"entity_name": "ETFA",
"entity_type": "gene"
},
{
"created": "2016-11-03T17:35:15.846000Z",
"panel_name": "Hyperammonaemia",
"panel_id": 267,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on DBT",
"entity_name": "DBT",
"entity_type": "gene"
},
{
"created": "2016-11-03T17:30:49.480000Z",
"panel_name": "Hyperammonaemia",
"panel_id": 267,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on BCKDHB",
"entity_name": "BCKDHB",
"entity_type": "gene"
},
{
"created": "2016-11-03T17:28:21.022000Z",
"panel_name": "Hyperammonaemia",
"panel_id": 267,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on BCKDHA",
"entity_name": "BCKDHA",
"entity_type": "gene"
},
{
"created": "2016-11-03T17:08:43.706000Z",
"panel_name": "Hyperammonaemia",
"panel_id": 267,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "edited their review of AUH",
"entity_name": "AUH",
"entity_type": "gene"
},
{
"created": "2016-11-03T17:07:56.324000Z",
"panel_name": "Hyperammonaemia",
"panel_id": 267,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked AUH as ready",
"entity_name": "AUH",
"entity_type": "gene"
},
{
"created": "2016-11-03T17:07:56.323000Z",
"panel_name": "Hyperammonaemia",
"panel_id": 267,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on AUH",
"entity_name": "AUH",
"entity_type": "gene"
},
{
"created": "2016-11-03T16:57:44.278000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked SLC41A1 as ready",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2016-11-03T16:57:40.821000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified SLC41A1 as red",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2016-11-03T16:57:40.820000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on SLC41A1",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2016-11-03T16:43:27.573000Z",
"panel_name": "Hyperammonaemia",
"panel_id": 267,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked ALDH18A1 as ready",
"entity_name": "ALDH18A1",
"entity_type": "gene"
},
{
"created": "2016-11-03T16:30:44.186000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified SLC30A10 as amber",
"entity_name": "SLC30A10",
"entity_type": "gene"
},
{
"created": "2016-11-03T16:30:44.185000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on SLC30A10",
"entity_name": "SLC30A10",
"entity_type": "gene"
},
{
"created": "2016-11-03T16:16:54.211000Z",
"panel_name": "Hyperammonaemia",
"panel_id": 267,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on ALDH18A1",
"entity_name": "ALDH18A1",
"entity_type": "gene"
},
{
"created": "2016-11-03T16:15:37.901000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "marked AR as ready",
"entity_name": "AR",
"entity_type": "gene"
},
{
"created": "2016-11-03T16:05:03.778000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified RAB39B as amber",
"entity_name": "RAB39B",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:59:43.816000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "marked UBE2T as ready",
"entity_name": "UBE2T",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:58:40.918000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "marked ERCC4 as ready",
"entity_name": "ERCC4",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:58:33.979000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified ERCC4 as red",
"entity_name": "ERCC4",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:56:04.309000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "marked RAD51C as ready",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:54:40.609000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "marked GNAS as ready",
"entity_name": "GNAS",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:54:04.865000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "marked FANCM as ready",
"entity_name": "FANCM",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:41:03.988000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified RAB39B as red",
"entity_name": "RAB39B",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:41:03.987000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on RAB39B",
"entity_name": "RAB39B",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:29:16.262000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PRKRA as amber",
"entity_name": "PRKRA",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:29:16.261000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on PRKRA",
"entity_name": "PRKRA",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:28:29.123000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PRKRA as amber",
"entity_name": "PRKRA",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:28:17.745000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "edited their review of PRKRA",
"entity_name": "PRKRA",
"entity_type": "gene"
},
{
"created": "2016-11-03T15:28:01.216000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "edited their review of PRKRA",
"entity_name": "PRKRA",
"entity_type": "gene"
},
{
"created": "2016-11-03T14:07:23.665000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked NR4A2 as ready",
"entity_name": "NR4A2",
"entity_type": "gene"
},
{
"created": "2016-11-03T14:00:07.292000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Rebecca Foulger",
"item_type": "panel",
"text": "promoted panel to version 1",
"entity_name": null,
"entity_type": null
},
{
"created": "2016-11-03T13:09:02.972000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified NR4A2 as red",
"entity_name": "NR4A2",
"entity_type": "gene"
},
{
"created": "2016-11-03T13:09:02.971000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on NR4A2",
"entity_name": "NR4A2",
"entity_type": "gene"
},
{
"created": "2016-11-03T12:54:41.409000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified GRN as amber",
"entity_name": "GRN",
"entity_type": "gene"
},
{
"created": "2016-11-03T12:54:41.408000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on GRN",
"entity_name": "GRN",
"entity_type": "gene"
},
{
"created": "2016-11-03T12:42:26.445000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified GNAL as amber",
"entity_name": "GNAL",
"entity_type": "gene"
},
{
"created": "2016-11-03T12:41:39.346000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked GIGYF2 as ready",
"entity_name": "GIGYF2",
"entity_type": "gene"
},
{
"created": "2016-11-03T12:41:04.551000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified GIGYF2 as red",
"entity_name": "GIGYF2",
"entity_type": "gene"
},
{
"created": "2016-11-03T12:41:04.550000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on GIGYF2",
"entity_name": "GIGYF2",
"entity_type": "gene"
},
{
"created": "2016-11-03T12:22:34.752000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Rebecca Foulger",
"item_type": "entity",
"text": "classified VANGL1 as red",
"entity_name": "VANGL1",
"entity_type": "gene"
},
{
"created": "2016-11-03T12:22:34.751000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Rebecca Foulger",
"item_type": "entity",
"text": "commented on VANGL1",
"entity_name": "VANGL1",
"entity_type": "gene"
},
{
"created": "2016-11-03T12:21:31.232000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Rebecca Foulger",
"item_type": "entity",
"text": "marked MNX1 as ready",
"entity_name": "MNX1",
"entity_type": "gene"
},
{
"created": "2016-11-03T12:01:58.505000Z",
"panel_name": "Posterior segment abnormalities",
"panel_id": 307,
"panel_version": null,
"user_name": "Ellen Thomas",
"item_type": "entity",
"text": "added AGBL5 to panel",
"entity_name": "AGBL5",
"entity_type": "gene"
},
{
"created": "2016-11-03T12:01:56.852000Z",
"panel_name": "Posterior segment abnormalities",
"panel_id": 307,
"panel_version": null,
"user_name": "Ellen Thomas",
"item_type": "entity",
"text": "reviewed AGBL5",
"entity_name": "AGBL5",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:57:01.866000Z",
"panel_name": "Cerebellar hypoplasia",
"panel_id": 286,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "added TSEN15 to panel",
"entity_name": "TSEN15",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:57:01.671000Z",
"panel_name": "Cerebellar hypoplasia",
"panel_id": 286,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed TSEN15",
"entity_name": "TSEN15",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:50:01.203000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked GBA as ready",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:48:17.315000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Richard Scott",
"item_type": "entity",
"text": "reviewed ZIC3",
"entity_name": "ZIC3",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:48:17.240000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Richard Scott",
"item_type": "entity",
"text": "reviewed VANGL2",
"entity_name": "VANGL2",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:48:17.167000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Richard Scott",
"item_type": "entity",
"text": "reviewed T",
"entity_name": "T",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:48:17.094000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Richard Scott",
"item_type": "entity",
"text": "reviewed SHH",
"entity_name": "SHH",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:48:17.020000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Richard Scott",
"item_type": "entity",
"text": "reviewed PCSK5",
"entity_name": "PCSK5",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:48:16.941000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Richard Scott",
"item_type": "entity",
"text": "reviewed PAM16",
"entity_name": "PAM16",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:48:16.862000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Richard Scott",
"item_type": "entity",
"text": "reviewed GDF6",
"entity_name": "GDF6",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:48:16.791000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Richard Scott",
"item_type": "entity",
"text": "reviewed GDF11",
"entity_name": "GDF11",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:48:16.718000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Richard Scott",
"item_type": "entity",
"text": "reviewed FUZ",
"entity_name": "FUZ",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:48:16.639000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Richard Scott",
"item_type": "entity",
"text": "reviewed VANGL1",
"entity_name": "VANGL1",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:48:16.564000Z",
"panel_name": "Currarino triad",
"panel_id": 5,
"panel_version": null,
"user_name": "Richard Scott",
"item_type": "entity",
"text": "reviewed MNX1",
"entity_name": "MNX1",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:47:54.754000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified GBA as red",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:47:54.753000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on GBA",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:40:45.754000Z",
"panel_name": "Cerebellar hypoplasia",
"panel_id": 286,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified VPS53 as amber",
"entity_name": "VPS53",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:38:26.863000Z",
"panel_name": "Cerebellar hypoplasia",
"panel_id": 286,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed VPS53",
"entity_name": "VPS53",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:35:32.444000Z",
"panel_name": "Cerebellar hypoplasia",
"panel_id": 286,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "marked SPTBN2 as ready",
"entity_name": "SPTBN2",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:35:32.443000Z",
"panel_name": "Cerebellar hypoplasia",
"panel_id": 286,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "commented on SPTBN2",
"entity_name": "SPTBN2",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:27:48.356000Z",
"panel_name": "Cerebellar hypoplasia",
"panel_id": 286,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "marked KCNC3 as ready",
"entity_name": "KCNC3",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:27:48.355000Z",
"panel_name": "Cerebellar hypoplasia",
"panel_id": 286,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "commented on KCNC3",
"entity_name": "KCNC3",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:19:31.581000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked EIF4G1 as ready",
"entity_name": "EIF4G1",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:19:27.062000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified EIF4G1 as red",
"entity_name": "EIF4G1",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:19:27.061000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on EIF4G1",
"entity_name": "EIF4G1",
"entity_type": "gene"
},
{
"created": "2016-11-03T11:19:08.657000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked TSPYL1 as ready",
"entity_name": "TSPYL1",
"entity_type": "gene"
}
]
}