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{
"created": "2016-08-24T13:43:20.052000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified SCP2 as green",
"entity_name": "SCP2",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:39:00.605000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked SCO2 as ready",
"entity_name": "SCO2",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:38:36.303000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on SCO2",
"entity_name": "SCO2",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:37:46.817000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified SCO2 as green",
"entity_name": "SCO2",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:33:30.681000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked SCO1 as ready",
"entity_name": "SCO1",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:33:30.680000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on SCO1",
"entity_name": "SCO1",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:32:03.326000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified SCO1 as green",
"entity_name": "SCO1",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:21:18.820000Z",
"panel_name": "Craniosynostosis syndromes phenotypes",
"panel_id": 168,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on EFNB1",
"entity_name": "EFNB1",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:11:46.716000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked RRM2B as ready",
"entity_name": "RRM2B",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:08:52.583000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified RRM2B as green",
"entity_name": "RRM2B",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:06:37.824000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on RRM2B",
"entity_name": "RRM2B",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:01:06.289000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked RNASET2 as ready",
"entity_name": "RNASET2",
"entity_type": "gene"
},
{
"created": "2016-08-24T13:01:06.288000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on RNASET2",
"entity_name": "RNASET2",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:59:13.203000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified RNASET2 as green",
"entity_name": "RNASET2",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:50:31.619000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on RARS",
"entity_name": "RARS",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:49:11.543000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified RARS as amber",
"entity_name": "RARS",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:44:36.415000Z",
"panel_name": "Hereditary ataxia",
"panel_id": 20,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on POLG",
"entity_name": "POLG",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:41:48.524000Z",
"panel_name": "Hereditary ataxia",
"panel_id": 20,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "commented on OPHN1",
"entity_name": "OPHN1",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:34:45.412000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked POLG2 as ready",
"entity_name": "POLG2",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:34:45.411000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on POLG2",
"entity_name": "POLG2",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:32:48.112000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified POLG2 as green",
"entity_name": "POLG2",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:24:02.420000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked POLG as ready",
"entity_name": "POLG",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:22:59.085000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on POLG",
"entity_name": "POLG",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:19:19.576000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified POLG as green",
"entity_name": "POLG",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:06:36.883000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified PEX5 as green",
"entity_name": "PEX5",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:06:16.235000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked PEX5 as ready",
"entity_name": "PEX5",
"entity_type": "gene"
},
{
"created": "2016-08-24T12:06:03.325000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked PEX5 as ready",
"entity_name": "PEX5",
"entity_type": "gene"
},
{
"created": "2016-08-24T11:58:12.190000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PEX5",
"entity_name": "PEX5",
"entity_type": "gene"
},
{
"created": "2016-08-24T10:58:44.282000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked PEX3 as ready",
"entity_name": "PEX3",
"entity_type": "gene"
},
{
"created": "2016-08-24T10:55:43.181000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked PEX3 as ready",
"entity_name": "PEX3",
"entity_type": "gene"
},
{
"created": "2016-08-24T10:55:43.180000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PEX3",
"entity_name": "PEX3",
"entity_type": "gene"
},
{
"created": "2016-08-24T10:54:07.519000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified PEX3 as green",
"entity_name": "PEX3",
"entity_type": "gene"
},
{
"created": "2016-08-24T10:43:42.016000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked PEX26 as ready",
"entity_name": "PEX26",
"entity_type": "gene"
},
{
"created": "2016-08-24T10:43:42.015000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PEX26",
"entity_name": "PEX26",
"entity_type": "gene"
},
{
"created": "2016-08-24T10:41:40.207000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified PEX26 as green",
"entity_name": "PEX26",
"entity_type": "gene"
},
{
"created": "2016-08-24T10:38:52.105000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PEX2",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2016-08-24T10:24:11.856000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified PEX2 as green",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2016-08-24T09:40:22.880000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified PEX19 as green",
"entity_name": "PEX19",
"entity_type": "gene"
},
{
"created": "2016-08-24T09:40:08.134000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "edited their review of PEX19",
"entity_name": "PEX19",
"entity_type": "gene"
},
{
"created": "2016-08-24T08:04:48.033000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified PEX11B as green",
"entity_name": "PEX11B",
"entity_type": "gene"
},
{
"created": "2016-08-24T08:04:01.281000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "edited their review of PEX11B",
"entity_name": "PEX11B",
"entity_type": "gene"
},
{
"created": "2016-08-24T07:39:04.444000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "edited their review of PEX11B",
"entity_name": "PEX11B",
"entity_type": "gene"
},
{
"created": "2016-08-24T07:38:33.405000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PEX19",
"entity_name": "PEX19",
"entity_type": "gene"
},
{
"created": "2016-08-24T07:36:44.191000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified PEX19 as amber",
"entity_name": "PEX19",
"entity_type": "gene"
},
{
"created": "2016-08-24T07:36:24.784000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "reviewed PEX19",
"entity_name": "PEX19",
"entity_type": "gene"
},
{
"created": "2016-08-24T07:20:24.362000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "edited their review of PEX11B",
"entity_name": "PEX11B",
"entity_type": "gene"
},
{
"created": "2016-08-24T07:18:03.418000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "reviewed PEX7",
"entity_name": "PEX7",
"entity_type": "gene"
},
{
"created": "2016-08-24T07:07:17.731000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked PEX6 as ready",
"entity_name": "PEX6",
"entity_type": "gene"
},
{
"created": "2016-08-24T07:05:48.090000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked PEX6 as ready",
"entity_name": "PEX6",
"entity_type": "gene"
},
{
"created": "2016-08-24T07:02:02.922000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PEX6",
"entity_name": "PEX6",
"entity_type": "gene"
},
{
"created": "2016-08-24T07:01:41.671000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "marked PEX6 as ready",
"entity_name": "PEX6",
"entity_type": "gene"
},
{
"created": "2016-08-24T06:58:10.963000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PEX6",
"entity_name": "PEX6",
"entity_type": "gene"
},
{
"created": "2016-08-24T06:50:27.291000Z",
"panel_name": "Inherited white matter disorders",
"panel_id": 42,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "classified PEX6 as green",
"entity_name": "PEX6",
"entity_type": "gene"
},
{
"created": "2016-08-23T15:18:24.753000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked SLC2A1 as ready",
"entity_name": "SLC2A1",
"entity_type": "gene"
},
{
"created": "2016-08-23T15:15:14.787000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified SLC2A1 as green",
"entity_name": "SLC2A1",
"entity_type": "gene"
},
{
"created": "2016-08-23T15:06:53.339000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked SGCE as ready",
"entity_name": "SGCE",
"entity_type": "gene"
},
{
"created": "2016-08-23T15:05:50.903000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified SGCE as green",
"entity_name": "SGCE",
"entity_type": "gene"
},
{
"created": "2016-08-23T15:00:04.091000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked PRRT2 as ready",
"entity_name": "PRRT2",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:50:17.645000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PRRT2 as green",
"entity_name": "PRRT2",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:44:55.268000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PNKD as green",
"entity_name": "PNKD",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:38:06.386000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked PLA2G6 as ready",
"entity_name": "PLA2G6",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:37:52.974000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PLA2G6 as green",
"entity_name": "PLA2G6",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:30:32.530000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PINK1 as green",
"entity_name": "PINK1",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:27:10.790000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "edited their review of PEX5",
"entity_name": "PEX5",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:25:37.193000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PEX5",
"entity_name": "PEX5",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:23:06.251000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PARK7 as green",
"entity_name": "PARK7",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:17:38.624000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked PARK2 as ready",
"entity_name": "PARK2",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:16:24.218000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PARK2 as green",
"entity_name": "PARK2",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:13:24.014000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked PANK2 as ready",
"entity_name": "PANK2",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:13:19.615000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PANK2 as green",
"entity_name": "PANK2",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:09:11.713000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified GCH1 as green",
"entity_name": "GCH1",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:03:37.697000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked FTL as ready",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:03:22.321000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "reviewed PEX3",
"entity_name": "PEX3",
"entity_type": "gene"
},
{
"created": "2016-08-23T14:03:10.678000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified FTL as green",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:58:28.640000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked FBXO7 as ready",
"entity_name": "FBXO7",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:58:19.834000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified FBXO7 as green",
"entity_name": "FBXO7",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:53:07.090000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked FA2H as ready",
"entity_name": "FA2H",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:52:45.699000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified FA2H as green",
"entity_name": "FA2H",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:52:44.999000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified FA2H as green",
"entity_name": "FA2H",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:46:28.931000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked DCAF17 as ready",
"entity_name": "DCAF17",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:45:40.016000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified DCAF17 as green",
"entity_name": "DCAF17",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:44:52.729000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "reviewed PEX26",
"entity_name": "PEX26",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:43:42.291000Z",
"panel_name": "Idiopathic hypogonadotropic hypogonadism",
"panel_id": 92,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "added DCAF17 to panel",
"entity_name": "DCAF17",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:43:41.919000Z",
"panel_name": "Idiopathic hypogonadotropic hypogonadism",
"panel_id": 92,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "reviewed DCAF17",
"entity_name": "DCAF17",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:31:09.763000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "reviewed PEX2",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:15:06.842000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "edited their review of PEX14",
"entity_name": "PEX14",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:14:47.294000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "edited their review of PEX16",
"entity_name": "PEX16",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:14:12.808000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "edited their review of PEX16",
"entity_name": "PEX16",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:13:56.073000Z",
"panel_name": "Early onset dystonia",
"panel_id": 192,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified COASY as green",
"entity_name": "COASY",
"entity_type": "gene"
},
{
"created": "2016-08-23T13:11:10.410000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PEX16",
"entity_name": "PEX16",
"entity_type": "gene"
},
{
"created": "2016-08-23T12:37:07.190000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "reviewed PEX13",
"entity_name": "PEX13",
"entity_type": "gene"
},
{
"created": "2016-08-23T12:09:32.364000Z",
"panel_name": "Diabetes with additional phenotypes suggestive of a monogenic aetiology",
"panel_id": 26,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked STAT1 as ready",
"entity_name": "STAT1",
"entity_type": "gene"
},
{
"created": "2016-08-23T12:09:19.346000Z",
"panel_name": "Diabetes with additional phenotypes suggestive of a monogenic aetiology",
"panel_id": 26,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified STAT1 as red",
"entity_name": "STAT1",
"entity_type": "gene"
},
{
"created": "2016-08-23T12:09:05.690000Z",
"panel_name": "Diabetes with additional phenotypes suggestive of a monogenic aetiology",
"panel_id": 26,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "added STAT1 to panel",
"entity_name": "STAT1",
"entity_type": "gene"
},
{
"created": "2016-08-23T12:09:05.200000Z",
"panel_name": "Diabetes with additional phenotypes suggestive of a monogenic aetiology",
"panel_id": 26,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "reviewed STAT1",
"entity_name": "STAT1",
"entity_type": "gene"
},
{
"created": "2016-08-23T12:07:53.174000Z",
"panel_name": "Diabetes with additional phenotypes suggestive of a monogenic aetiology",
"panel_id": 26,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "marked PCBD1 as ready",
"entity_name": "PCBD1",
"entity_type": "gene"
},
{
"created": "2016-08-23T12:07:46.687000Z",
"panel_name": "Diabetes with additional phenotypes suggestive of a monogenic aetiology",
"panel_id": 26,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "classified PCBD1 as red",
"entity_name": "PCBD1",
"entity_type": "gene"
},
{
"created": "2016-08-23T12:07:21.352000Z",
"panel_name": "Diabetes with additional phenotypes suggestive of a monogenic aetiology",
"panel_id": 26,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "added PCBD1 to panel",
"entity_name": "PCBD1",
"entity_type": "gene"
},
{
"created": "2016-08-23T12:07:20.860000Z",
"panel_name": "Diabetes with additional phenotypes suggestive of a monogenic aetiology",
"panel_id": 26,
"panel_version": null,
"user_name": "Ellen McDonagh",
"item_type": "entity",
"text": "reviewed PCBD1",
"entity_name": "PCBD1",
"entity_type": "gene"
},
{
"created": "2016-08-23T12:05:37.133000Z",
"panel_name": "Peroxisomal disorders",
"panel_id": 114,
"panel_version": null,
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on PEX1",
"entity_name": "PEX1",
"entity_type": "gene"
}
]
}