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{
"count": 216110,
"next": "https://panelapp.genomicsengland.co.uk/api/v1/activities/?format=api&page=2137",
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"results": [
{
"created": "2016-11-02T13:47:22.414000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked PLA2G6 as ready",
"entity_name": "PLA2G6",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:47:18.989000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified TSPYL1 as amber",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:46:59.792000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PLA2G6 as green",
"entity_name": "PLA2G6",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:46:47.602000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on TSPYL1",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:46:47.602000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified TSPYL1 as green",
"entity_name": "TSPYL1",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:42:44.296000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked PINK1 as ready",
"entity_name": "PINK1",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:42:11.183000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PINK1 as green",
"entity_name": "PINK1",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:39:04.684000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified CHCHD10 as red",
"entity_name": "CHCHD10",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:39:04.683000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "commented on CHCHD10",
"entity_name": "CHCHD10",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:37:53.147000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked PARK7 as ready",
"entity_name": "PARK7",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:37:51.709000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified BSCL2 as red",
"entity_name": "BSCL2",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:37:51.708000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "commented on BSCL2",
"entity_name": "BSCL2",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:37:24.319000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PARK7 as green",
"entity_name": "PARK7",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:35:53.499000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "commented on BICD2",
"entity_name": "BICD2",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:35:53.499000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified BICD2 as red",
"entity_name": "BICD2",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:34:53.923000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified ATP7A as red",
"entity_name": "ATP7A",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:34:53.922000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "commented on ATP7A",
"entity_name": "ATP7A",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:34:47.413000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked PARK2 as ready",
"entity_name": "PARK2",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:34:42.293000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PARK2 as green",
"entity_name": "PARK2",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:32:46.701000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "commented on AARS",
"entity_name": "AARS",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:32:46.701000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified AARS as red",
"entity_name": "AARS",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:32:31.711000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked PANK2 as ready",
"entity_name": "PANK2",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:30:29.233000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PANK2 as green",
"entity_name": "PANK2",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:27:47.311000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified TRPV4 as red",
"entity_name": "TRPV4",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:27:47.310000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "commented on TRPV4",
"entity_name": "TRPV4",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:27:10.816000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked MAPT as ready",
"entity_name": "MAPT",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:25:00.587000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified PLEKHG5 as red",
"entity_name": "PLEKHG5",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:25:00.586000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "commented on PLEKHG5",
"entity_name": "PLEKHG5",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:24:17.720000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified MAPT as green",
"entity_name": "MAPT",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:20:57.540000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified AR as green",
"entity_name": "AR",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:20:57.538000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "commented on AR",
"entity_name": "AR",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:16:53.864000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked TAF4B as ready",
"entity_name": "TAF4B",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:14:47.394000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked MAP3K1 as ready",
"entity_name": "MAP3K1",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:13:49.189000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified MAP3K1 as green",
"entity_name": "MAP3K1",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:13:49.188000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on MAP3K1",
"entity_name": "MAP3K1",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:13:25.983000Z",
"panel_name": "Parkinson Disease and Complex Parkinsonism",
"panel_id": 39,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified LRRK2 as amber",
"entity_name": "LRRK2",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:11:15.673000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked HSD17B2 as ready",
"entity_name": "HSD17B2",
"entity_type": "gene"
},
{
"created": "2016-11-02T13:11:15.672000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on HSD17B2",
"entity_name": "HSD17B2",
"entity_type": "gene"
},
{
"created": "2016-11-02T12:59:53.976000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "added ALS2 to panel",
"entity_name": "ALS2",
"entity_type": "gene"
},
{
"created": "2016-11-02T12:59:53.795000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed ALS2",
"entity_name": "ALS2",
"entity_type": "gene"
},
{
"created": "2016-11-02T12:48:28.681000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked HHAT as ready",
"entity_name": "HHAT",
"entity_type": "gene"
},
{
"created": "2016-11-02T12:48:28.679000Z",
"panel_name": "Disorders of sex development",
"panel_id": 9,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on HHAT",
"entity_name": "HHAT",
"entity_type": "gene"
},
{
"created": "2016-11-02T12:16:56.219000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified IGHMBP2 as green",
"entity_name": "IGHMBP2",
"entity_type": "gene"
},
{
"created": "2016-11-02T12:16:56.218000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "commented on IGHMBP2",
"entity_name": "IGHMBP2",
"entity_type": "gene"
},
{
"created": "2016-11-02T12:10:52.055000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed SMN1",
"entity_name": "SMN1",
"entity_type": "gene"
},
{
"created": "2016-11-02T12:03:41.663000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed SLC52A1",
"entity_name": "SLC52A1",
"entity_type": "gene"
},
{
"created": "2016-11-02T12:01:36.196000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed SLC52A1",
"entity_name": "SLC52A1",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:54:26.717000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified SLC52A2 as green",
"entity_name": "SLC52A2",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:54:11.294000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed SLC52A2",
"entity_name": "SLC52A2",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:50:15.959000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified SLC52A3 as green",
"entity_name": "SLC52A3",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:49:56.985000Z",
"panel_name": "Paediatric motor neuronopathies",
"panel_id": 79,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed SLC52A3",
"entity_name": "SLC52A3",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:17:56.732000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked CDC42 as ready",
"entity_name": "CDC42",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:17:56.731000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on CDC42",
"entity_name": "CDC42",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:16:53.036000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "added UBE2T to panel",
"entity_name": "UBE2T",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:16:52.806000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed UBE2T",
"entity_name": "UBE2T",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:10:32.601000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed SLX4",
"entity_name": "SLX4",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:07:46.014000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed PALB2",
"entity_name": "PALB2",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:07:29.948000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked VEGFC as ready",
"entity_name": "VEGFC",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:07:29.946000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on VEGFC",
"entity_name": "VEGFC",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:04:23.156000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed FANCM",
"entity_name": "FANCM",
"entity_type": "gene"
},
{
"created": "2016-11-02T11:02:07.661000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked SOX18 as ready",
"entity_name": "SOX18",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:58:23.742000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked PIEZO1 as ready",
"entity_name": "PIEZO1",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:58:21.318000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed FANCL",
"entity_name": "FANCL",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:57:45.040000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PIEZO1",
"entity_name": "PIEZO1",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:54:14.078000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked KIF11 as ready",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:54:14.077000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on KIF11",
"entity_name": "KIF11",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:53:08.985000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed ERCC4",
"entity_name": "ERCC4",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:52:48.911000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked IKBKG as ready",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:50:27.206000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on IKBKG",
"entity_name": "IKBKG",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:48:19.554000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed RAD51C",
"entity_name": "RAD51C",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:44:29.564000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked GJC2 as ready",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:39:48.241000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on GJC2",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:35:11.283000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked GATA2 as ready",
"entity_name": "GATA2",
"entity_type": "gene"
},
{
"created": "2016-11-02T10:28:53.821000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on GATA2",
"entity_name": "GATA2",
"entity_type": "gene"
},
{
"created": "2016-11-02T09:42:38.796000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "added PMS2 to panel",
"entity_name": "PMS2",
"entity_type": "gene"
},
{
"created": "2016-11-02T09:42:38.715000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed PMS2",
"entity_name": "PMS2",
"entity_type": "gene"
},
{
"created": "2016-11-02T09:39:54.740000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "added MSH6 to panel",
"entity_name": "MSH6",
"entity_type": "gene"
},
{
"created": "2016-11-02T09:39:54.669000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed MSH6",
"entity_name": "MSH6",
"entity_type": "gene"
},
{
"created": "2016-11-02T09:36:48.759000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "added MSH2 to panel",
"entity_name": "MSH2",
"entity_type": "gene"
},
{
"created": "2016-11-02T09:36:48.696000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed MSH2",
"entity_name": "MSH2",
"entity_type": "gene"
},
{
"created": "2016-11-02T09:35:21.021000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on GJA1",
"entity_name": "GJA1",
"entity_type": "gene"
},
{
"created": "2016-11-02T09:34:00.318000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified SPRED1 as green",
"entity_name": "SPRED1",
"entity_type": "gene"
},
{
"created": "2016-11-02T09:33:42.971000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "classified GNAS as green",
"entity_name": "GNAS",
"entity_type": "gene"
},
{
"created": "2016-11-02T09:33:03.086000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "added MLH1 to panel",
"entity_name": "MLH1",
"entity_type": "gene"
},
{
"created": "2016-11-02T09:33:03.032000Z",
"panel_name": "Neurofibromatosis Type 1",
"panel_id": 255,
"panel_version": null,
"user_name": "Alice Gardham",
"item_type": "entity",
"text": "reviewed MLH1",
"entity_name": "MLH1",
"entity_type": "gene"
},
{
"created": "2016-11-02T08:25:32.458000Z",
"panel_name": "Cerebrovascular disorders",
"panel_id": 147,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "panel",
"text": "approved panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2016-11-01T17:03:17.674000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked CCDC88A as ready",
"entity_name": "CCDC88A",
"entity_type": "gene"
},
{
"created": "2016-11-01T17:03:17.673000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on CCDC88A",
"entity_name": "CCDC88A",
"entity_type": "gene"
},
{
"created": "2016-11-01T16:53:11.017000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked AQP1 as ready",
"entity_name": "AQP1",
"entity_type": "gene"
},
{
"created": "2016-11-01T16:52:22.515000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on AQP1",
"entity_name": "AQP1",
"entity_type": "gene"
},
{
"created": "2016-11-01T16:15:11.742000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked ALX3 as ready",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2016-11-01T16:11:00.986000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on ALX3",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2016-11-01T16:11:00.986000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified ALX3 as red",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2016-11-01T16:08:12.960000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked PTPN14 as ready",
"entity_name": "PTPN14",
"entity_type": "gene"
},
{
"created": "2016-11-01T16:08:12.958000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PTPN14",
"entity_name": "PTPN14",
"entity_type": "gene"
},
{
"created": "2016-11-01T16:02:44.092000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked TTR as ready",
"entity_name": "TTR",
"entity_type": "gene"
},
{
"created": "2016-11-01T16:01:27.593000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified TTR as red",
"entity_name": "TTR",
"entity_type": "gene"
},
{
"created": "2016-11-01T16:01:27.593000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on TTR",
"entity_name": "TTR",
"entity_type": "gene"
},
{
"created": "2016-11-01T15:51:56.871000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Pia Ostergaard",
"item_type": "entity",
"text": "commented on PTPN14",
"entity_name": "PTPN14",
"entity_type": "gene"
},
{
"created": "2016-11-01T15:51:56.791000Z",
"panel_name": "Lymphatic Disorders",
"panel_id": 65,
"panel_version": null,
"user_name": "Pia Ostergaard",
"item_type": "entity",
"text": "reviewed TTR",
"entity_name": "TTR",
"entity_type": "gene"
}
]
}