GET /api/v1/activities/?format=api&page=2137
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{
    "count": 216020,
    "next": "https://panelapp.genomicsengland.co.uk/api/v1/activities/?format=api&page=2138",
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    "results": [
        {
            "created": "2016-10-26T15:20:28.375000Z",
            "panel_name": "Lymphatic Disorders",
            "panel_id": 65,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "commented on EPHB4",
            "entity_name": "EPHB4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-26T09:48:58.860000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "panel",
            "text": "promoted panel to version 1",
            "entity_name": null,
            "entity_type": null
        },
        {
            "created": "2016-10-26T09:30:16.715000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified SALL4 as green",
            "entity_name": "SALL4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-26T07:49:50.132000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified HOXA2 as green",
            "entity_name": "HOXA2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-26T07:49:41.436000Z",
            "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": "2016-10-26T07:25:56.909000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "panel",
            "text": "promoted panel to version 1",
            "entity_name": null,
            "entity_type": null
        },
        {
            "created": "2016-10-26T04:06:44.964000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified KDM6A as green",
            "entity_name": "KDM6A",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-26T04:06:32.874000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified KMT2D as green",
            "entity_name": "KMT2D",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-26T04:05:59.164000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "reviewed KDM6A",
            "entity_name": "KDM6A",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-26T04:05:03.469000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "reviewed KMT2D",
            "entity_name": "KMT2D",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-26T04:02:15.987000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "marked HSPA9 as ready",
            "entity_name": "HSPA9",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-26T04:02:04.852000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified HSPA9 as green",
            "entity_name": "HSPA9",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-26T04:00:09.586000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "added HSPA9 to panel",
            "entity_name": "HSPA9",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-26T04:00:08.956000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "reviewed HSPA9",
            "entity_name": "HSPA9",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:18:03.013000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified SALL4 as amber",
            "entity_name": "SALL4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:18:03.010000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on SALL4",
            "entity_name": "SALL4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:14:10.016000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified BMP4 as green",
            "entity_name": "BMP4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:12:56.846000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified BMP4 as green",
            "entity_name": "BMP4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:10:53.349000Z",
            "panel_name": "Deafness and congenital structural abnormalities",
            "panel_id": 251,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "reviewed BMP4",
            "entity_name": "BMP4",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:10:17.444000Z",
            "panel_name": "Multiple lipomas",
            "panel_id": 19,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "added MT-TK to panel",
            "entity_name": "MT-TK",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:10:17.428000Z",
            "panel_name": "Multiple lipomas",
            "panel_id": 19,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "reviewed MT-TK",
            "entity_name": "MT-TK",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:04:14.255000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified SCN11A as green",
            "entity_name": "SCN11A",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:04:14.254000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on SCN11A",
            "entity_name": "SCN11A",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:01:32.376000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified RRM2B as green",
            "entity_name": "RRM2B",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:01:32.375000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on RRM2B",
            "entity_name": "RRM2B",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:00:05.056000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified RET as green",
            "entity_name": "RET",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T16:00:05.055000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on RET",
            "entity_name": "RET",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:56:22.980000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified L1CAM as amber",
            "entity_name": "L1CAM",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:56:22.978000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on L1CAM",
            "entity_name": "L1CAM",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:53:30.176000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified EVC2 as red",
            "entity_name": "EVC2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:53:14.683000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified EVC2 as green",
            "entity_name": "EVC2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:53:14.683000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on EVC2",
            "entity_name": "EVC2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:49:58.301000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "classified DMD as green",
            "entity_name": "DMD",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:49:58.300000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Richard Scott",
            "item_type": "entity",
            "text": "commented on DMD",
            "entity_name": "DMD",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:27:16.263000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "panel",
            "text": "promoted panel to version 1",
            "entity_name": null,
            "entity_type": null
        },
        {
            "created": "2016-10-25T15:26:21.441000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified ZIC2 as red",
            "entity_name": "ZIC2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:26:14.013000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified VANGL1 as red",
            "entity_name": "VANGL1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:26:07.106000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TMEM67 as red",
            "entity_name": "TMEM67",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:25:59.506000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified RPGRIP1L as red",
            "entity_name": "RPGRIP1L",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:25:52.516000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified MTHFR as red",
            "entity_name": "MTHFR",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:25:45.327000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified LFNG as red",
            "entity_name": "LFNG",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:25:37.653000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified HES7 as red",
            "entity_name": "HES7",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:25:29.597000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified GDF6 as red",
            "entity_name": "GDF6",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:25:22.250000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CDON as red",
            "entity_name": "CDON",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:25:14.298000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CC2D2A as red",
            "entity_name": "CC2D2A",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:25:06.767000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TMEM216 as red",
            "entity_name": "TMEM216",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:25:00.156000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TCTN2 as red",
            "entity_name": "TCTN2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:24:59.633000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TCTN2 as red",
            "entity_name": "TCTN2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:24:52.200000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified NPHP3 as red",
            "entity_name": "NPHP3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:24:45.367000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified MKS1 as red",
            "entity_name": "MKS1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:24:37.939000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified DLL3 as red",
            "entity_name": "DLL3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:24:30.641000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CEP290 as red",
            "entity_name": "CEP290",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:24:22.233000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified B9D2 as red",
            "entity_name": "B9D2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:24:14.553000Z",
            "panel_name": "Familial Neural Tube Defects",
            "panel_id": 11,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified B9D1 as red",
            "entity_name": "B9D1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-25T15:12:19.419000Z",
            "panel_name": "Significant early-onset obesity +/- other endocrine features and short stature",
            "panel_id": 130,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "panel",
            "text": "promoted panel to version 1",
            "entity_name": null,
            "entity_type": null
        },
        {
            "created": "2016-10-24T08:04:37.497000Z",
            "panel_name": "Currarino triad",
            "panel_id": 5,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "commented on SHH",
            "entity_name": "SHH",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-24T08:03:39.711000Z",
            "panel_name": "Currarino triad",
            "panel_id": 5,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "edited their review of MNX1",
            "entity_name": "MNX1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-24T08:03:07.390000Z",
            "panel_name": "Currarino triad",
            "panel_id": 5,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "commented on GDF11",
            "entity_name": "GDF11",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-24T08:01:40.841000Z",
            "panel_name": "Currarino triad",
            "panel_id": 5,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "commented on PCSK5",
            "entity_name": "PCSK5",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-24T07:57:06.890000Z",
            "panel_name": "Currarino triad",
            "panel_id": 5,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "classified MNX1 as green",
            "entity_name": "MNX1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-24T07:57:06.888000Z",
            "panel_name": "Currarino triad",
            "panel_id": 5,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "commented on MNX1",
            "entity_name": "MNX1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-24T07:41:28.031000Z",
            "panel_name": "Currarino triad",
            "panel_id": 5,
            "panel_version": null,
            "user_name": "Rebecca Foulger",
            "item_type": "entity",
            "text": "classified MNX1 as green",
            "entity_name": "MNX1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:59:13.050000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "panel",
            "text": "approved panel",
            "entity_name": null,
            "entity_type": null
        },
        {
            "created": "2016-10-19T14:57:22.336000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SNCA as green",
            "entity_name": "SNCA",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:55:29.305000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TAF1 as amber",
            "entity_name": "TAF1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:55:12.923000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified GNAL as amber",
            "entity_name": "GNAL",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:54:43.049000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified WDR45 as green",
            "entity_name": "WDR45",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:54:29.530000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified VPS35 as green",
            "entity_name": "VPS35",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:54:16.969000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TUBB4A as green",
            "entity_name": "TUBB4A",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:54:00.248000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TOR1A as green",
            "entity_name": "TOR1A",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:53:40.706000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified THAP1 as green",
            "entity_name": "THAP1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:53:27.185000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TH as green",
            "entity_name": "TH",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:53:12.837000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SPR as green",
            "entity_name": "SPR",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:51:07.750000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SLC6A3 as green",
            "entity_name": "SLC6A3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:31:35.824000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SGCE as green",
            "entity_name": "SGCE",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:31:21.789000Z",
            "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": "2016-10-19T14:30:57.670000Z",
            "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": "2016-10-19T14:30:41.163000Z",
            "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": "2016-10-19T14:30:22.613000Z",
            "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": "2016-10-19T14:30:01.651000Z",
            "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": "2016-10-19T14:29:36.064000Z",
            "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": "2016-10-19T14:29:17.650000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified LRRK2 as green",
            "entity_name": "LRRK2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:28:47.360000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified GCH1 as green",
            "entity_name": "GCH1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:28:22.449000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified FBXO7 as green",
            "entity_name": "FBXO7",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:28:01.256000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified DCTN1 as green",
            "entity_name": "DCTN1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:27:39.741000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified C19orf12 as green",
            "entity_name": "C19orf12",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:27:20.527000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified ATP1A3 as green",
            "entity_name": "ATP1A3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:26:58.376000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified ATP13A2 as green",
            "entity_name": "ATP13A2",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T14:26:33.460000Z",
            "panel_name": "Parkinson Disease and Complex Parkinsonism",
            "panel_id": 39,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified ANO3 as green",
            "entity_name": "ANO3",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T13:32:20.094000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "edited their review of PTEN",
            "entity_name": "PTEN",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T13:21:45.305000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on PTEN",
            "entity_name": "PTEN",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T13:21:45.305000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified PTEN as amber",
            "entity_name": "PTEN",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T13:17:25.831000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "edited their review of SOX10",
            "entity_name": "SOX10",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T13:16:58.411000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SOX10 as green",
            "entity_name": "SOX10",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T13:16:58.410000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on SOX10",
            "entity_name": "SOX10",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T13:12:13.708000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "edited their review of SMO",
            "entity_name": "SMO",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T13:04:38.419000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SMO as red",
            "entity_name": "SMO",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T13:04:38.418000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on SMO",
            "entity_name": "SMO",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T13:00:05.802000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "edited their review of SGOL1",
            "entity_name": "SGOL1",
            "entity_type": "gene"
        },
        {
            "created": "2016-10-19T12:55:58.255000Z",
            "panel_name": "Neonatal and familial gastrointestinal neuromuscular disorders",
            "panel_id": 61,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified SGOL1 as red",
            "entity_name": "SGOL1",
            "entity_type": "gene"
        }
    ]
}