GET /api/v1/activities/?page=1754
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{
    "count": 177481,
    "next": "https://panelapp.genomicsengland.co.uk/api/v1/activities/?page=1755",
    "previous": "https://panelapp.genomicsengland.co.uk/api/v1/activities/?page=1753",
    "results": [
        {
            "created": "2016-10-14T13:34:32.545000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked OTX2 as ready",
            "entity_name": "OTX2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T13:34:12.711000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified OTX2 as green",
            "entity_name": "OTX2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T13:31:57.776000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked NKX3-2 as ready",
            "entity_name": "NKX3-2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T13:31:51.563000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified NKX3-2 as red",
            "entity_name": "NKX3-2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T13:31:14.569000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked LEMD3 as ready",
            "entity_name": "LEMD3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T13:30:17.520000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified LEMD3 as red",
            "entity_name": "LEMD3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T13:28:35.802000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified KMT2D as amber",
            "entity_name": "KMT2D",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T13:21:48.397000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified HOXA2 as amber",
            "entity_name": "HOXA2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T13:20:04.712000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified GDF6 as amber",
            "entity_name": "GDF6",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T13:16:31.995000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked BMP5 as ready",
            "entity_name": "BMP5",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T13:16:27.973000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified BMP5 as red",
            "entity_name": "BMP5",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T13:04:41.209000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified BMP4 as green",
            "entity_name": "BMP4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:59:20.138000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SOX10 as green",
            "entity_name": "SOX10",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:59:20.136000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on SOX10",
            "entity_name": "SOX10",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:48:05.630000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SLC26A4 as green",
            "entity_name": "SLC26A4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:48:05.629000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on SLC26A4",
            "entity_name": "SLC26A4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:22:36.444000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SALL4 as amber",
            "entity_name": "SALL4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:22:36.443000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on SALL4",
            "entity_name": "SALL4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:17:23.061000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked RPS28 as ready",
            "entity_name": "RPS28",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:17:11.065000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified RPS28 as amber",
            "entity_name": "RPS28",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:14:35.825000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked POLR1A as ready",
            "entity_name": "POLR1A",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:14:21.675000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified POLR1A as green",
            "entity_name": "POLR1A",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:09:50.463000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified OFD1 as green",
            "entity_name": "OFD1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:09:50.462000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on OFD1",
            "entity_name": "OFD1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T12:07:02.125000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified FOXI1 as red",
            "entity_name": "FOXI1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:59:41.050000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked EIF4A3 as ready",
            "entity_name": "EIF4A3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:52:46.441000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified EIF4A3 as green",
            "entity_name": "EIF4A3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:52:38.161000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified EIF4A3 as red",
            "entity_name": "EIF4A3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:47:28.298000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked FGF10 as ready",
            "entity_name": "FGF10",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:44:26.081000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked EYA1 as ready",
            "entity_name": "EYA1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:44:23.232000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified EYA1 as green",
            "entity_name": "EYA1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:42:53.490000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified EFTUD2 as green",
            "entity_name": "EFTUD2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:42:33.685000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked EFTUD2 as ready",
            "entity_name": "EFTUD2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:37:12.159000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified EDNRA as green",
            "entity_name": "EDNRA",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:35:14.973000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked DHODH as ready",
            "entity_name": "DHODH",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:34:42.203000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified DHODH as green",
            "entity_name": "DHODH",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:23:10.024000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked CHD7 as ready",
            "entity_name": "CHD7",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:20:12.140000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CHD7 as green",
            "entity_name": "CHD7",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:16:21.544000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked CDT1 as ready",
            "entity_name": "CDT1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:16:17.894000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CDT1 as green",
            "entity_name": "CDT1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:08:32.940000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked CDC6 as ready",
            "entity_name": "CDC6",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:08:12.017000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CDC6 as green",
            "entity_name": "CDC6",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:05:27.562000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked EDNRA as ready",
            "entity_name": "EDNRA",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T11:04:12.848000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified EDNRA as green",
            "entity_name": "EDNRA",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:58:31.672000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "panel",
            "text": "promoted panel to version 1",
            "entity_name": null,
            "entity_type": null
        },
        {
            "created": "2016-10-14T10:52:22.502000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked FREM2 as ready",
            "entity_name": "FREM2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:52:08.156000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified FREM2 as green",
            "entity_name": "FREM2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:48:23.547000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked FRAS1 as ready",
            "entity_name": "FRAS1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:47:55.547000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified FRAS1 as green",
            "entity_name": "FRAS1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:46:48.618000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified FRAS1 as green",
            "entity_name": "FRAS1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:30:01.010000Z",
            "panel_name": "Idiopathic hypogonadotropic hypogonadism",
            "panel_id": 92,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "marked DCAF17 as ready",
            "entity_name": "DCAF17",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:30:01.009000Z",
            "panel_name": "Idiopathic hypogonadotropic hypogonadism",
            "panel_id": 92,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "commented on DCAF17",
            "entity_name": "DCAF17",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:23:01.271000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked TGFBR2 as ready",
            "entity_name": "TGFBR2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:22:58.691000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TGFBR2 as green",
            "entity_name": "TGFBR2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:22:36.792000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked TGFBR1 as ready",
            "entity_name": "TGFBR1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:22:33.956000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TGFBR1 as green",
            "entity_name": "TGFBR1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T10:17:21.228000Z",
            "panel_name": "Idiopathic hypogonadotropic hypogonadism",
            "panel_id": 92,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "classified SOX2 as green",
            "entity_name": "SOX2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T08:00:01.880000Z",
            "panel_name": "Intellectual disability",
            "panel_id": 285,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified SYNE1 as red",
            "entity_name": "SYNE1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T08:00:00.316000Z",
            "panel_name": "Intellectual disability",
            "panel_id": 285,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified SYNE1 as red",
            "entity_name": "SYNE1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T07:59:55.367000Z",
            "panel_name": "Intellectual disability",
            "panel_id": 285,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified SYNE1 as red",
            "entity_name": "SYNE1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T07:59:51.206000Z",
            "panel_name": "Intellectual disability",
            "panel_id": 285,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified SYNE1 as red",
            "entity_name": "SYNE1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T07:59:51.201000Z",
            "panel_name": "Intellectual disability",
            "panel_id": 285,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on SYNE1",
            "entity_name": "SYNE1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-14T07:49:08.531000Z",
            "panel_name": "Idiopathic hypogonadotropic hypogonadism",
            "panel_id": 92,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "classified SLC29A3 as green",
            "entity_name": "SLC29A3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:57:34.242000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified TGFBR2 as red",
            "entity_name": "TGFBR2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:57:34.241000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on TGFBR2",
            "entity_name": "TGFBR2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:57:16.648000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified TGFBR1 as red",
            "entity_name": "TGFBR1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:57:16.647000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on TGFBR1",
            "entity_name": "TGFBR1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:56:08.164000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified STAT1 as green",
            "entity_name": "STAT1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:56:08.163000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on STAT1",
            "entity_name": "STAT1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:53:35.935000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on RTEL1",
            "entity_name": "RTEL1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:53:35.935000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified RTEL1 as green",
            "entity_name": "RTEL1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:51:26.160000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified RAG1 as green",
            "entity_name": "RAG1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:51:26.158000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on RAG1",
            "entity_name": "RAG1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:50:52.962000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified G6PC3 as green",
            "entity_name": "G6PC3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T20:50:52.961000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on G6PC3",
            "entity_name": "G6PC3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T16:07:55.481000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TTC7A as red",
            "entity_name": "TTC7A",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T16:07:55.480000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on TTC7A",
            "entity_name": "TTC7A",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T16:06:10.837000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified PTRF as red",
            "entity_name": "PTRF",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T16:06:10.832000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on PTRF",
            "entity_name": "PTRF",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T16:04:41.986000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified COG7 as red",
            "entity_name": "COG7",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T16:04:41.985000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on COG7",
            "entity_name": "COG7",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T15:43:00.869000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified NCF4 as red",
            "entity_name": "NCF4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T15:42:23.624000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified NCF4 as amber",
            "entity_name": "NCF4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T15:42:23.623000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on NCF4",
            "entity_name": "NCF4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T15:19:54.826000Z",
            "panel_name": "Idiopathic hypogonadotropic hypogonadism",
            "panel_id": 92,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "marked FLRT3 as ready",
            "entity_name": "FLRT3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T15:09:40.790000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified NCF4 as amber",
            "entity_name": "NCF4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:52:54.294000Z",
            "panel_name": "Idiopathic hypogonadotropic hypogonadism",
            "panel_id": 92,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "classified SEMA3E as red",
            "entity_name": "SEMA3E",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:49:13.072000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TGFBR2 as amber",
            "entity_name": "TGFBR2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:49:13.070000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on TGFBR2",
            "entity_name": "TGFBR2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:47:31.155000Z",
            "panel_name": "Idiopathic hypogonadotropic hypogonadism",
            "panel_id": 92,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "classified LHX4 as green",
            "entity_name": "LHX4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:47:04.422000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on TGFBR1",
            "entity_name": "TGFBR1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:47:04.422000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TGFBR1 as amber",
            "entity_name": "TGFBR1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:42:08.313000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked STAT3 as ready",
            "entity_name": "STAT3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:40:33.149000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified STAT3 as green",
            "entity_name": "STAT3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:34:20.105000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on STAT1",
            "entity_name": "STAT1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:34:20.105000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified STAT1 as amber",
            "entity_name": "STAT1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:27:51.971000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified RTEL1 as amber",
            "entity_name": "RTEL1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T14:27:51.970000Z",
            "panel_name": "Infantile enterocolitis & monogenic inflammatory bowel disease",
            "panel_id": 176,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on RTEL1",
            "entity_name": "RTEL1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T13:35:23.647000Z",
            "panel_name": "Congenital hypothyroidism or thyroid agenesis",
            "panel_id": 31,
            "panel_version": null,
            "user_name": "Olivia Niblock",
            "item_type": "entity",
            "text": "reviewed FOXE1",
            "entity_name": "FOXE1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-13T13:32:48.928000Z",
            "panel_name": "Congenital hypothyroidism or thyroid agenesis",
            "panel_id": 31,
            "panel_version": null,
            "user_name": "Olivia Niblock",
            "item_type": "entity",
            "text": "added THRA to panel",
            "entity_name": "THRA",
            "entity_type": "gene"
        }
    ]
}