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    "results": [
        {
            "created": "2016-08-27T10:28:45.376000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked KIAA0586 as ready",
            "entity_name": "KIAA0586",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:28:25.366000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified KIAA0586 as green",
            "entity_name": "KIAA0586",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:28:25.365000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on KIAA0586",
            "entity_name": "KIAA0586",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:24:29.162000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked INPP5E as ready",
            "entity_name": "INPP5E",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:23:51.328000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified INPP5E as green",
            "entity_name": "INPP5E",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:23:51.327000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on INPP5E",
            "entity_name": "INPP5E",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:21:19.461000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked CSPP1 as ready",
            "entity_name": "CSPP1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:20:50.716000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CSPP1 as green",
            "entity_name": "CSPP1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:20:50.715000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on CSPP1",
            "entity_name": "CSPP1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:17:40.997000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked CEP41 as ready",
            "entity_name": "CEP41",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:17:19.923000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on CEP41",
            "entity_name": "CEP41",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:17:19.923000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CEP41 as green",
            "entity_name": "CEP41",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:14:48.740000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked CEP290 as ready",
            "entity_name": "CEP290",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:13:40.748000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CEP290 as green",
            "entity_name": "CEP290",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:07:35.356000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked CC2D2A as ready",
            "entity_name": "CC2D2A",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:06:27.908000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified CC2D2A as green",
            "entity_name": "CC2D2A",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T10:00:04.137000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked C5orf42 as ready",
            "entity_name": "C5orf42",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T09:59:32.089000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified C5orf42 as green",
            "entity_name": "C5orf42",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T09:59:32.088000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on C5orf42",
            "entity_name": "C5orf42",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T09:53:31.514000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked ARL13B as ready",
            "entity_name": "ARL13B",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T09:52:42.732000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified ARL13B as green",
            "entity_name": "ARL13B",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T09:52:42.731000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on ARL13B",
            "entity_name": "ARL13B",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T09:50:14.187000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked AHI1 as ready",
            "entity_name": "AHI1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-27T09:49:21.596000Z",
            "panel_name": "Rare multisystem ciliopathy disorders",
            "panel_id": 150,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified AHI1 as green",
            "entity_name": "AHI1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T14:44:12.302000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "added SCN11A to panel",
            "entity_name": "SCN11A",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T14:44:12.230000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "reviewed SCN11A",
            "entity_name": "SCN11A",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T14:17:22.670000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "edited their review of KIF1A",
            "entity_name": "KIF1A",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T13:33:39.798000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "added KIF1A to panel",
            "entity_name": "KIF1A",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T13:33:39.737000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "reviewed KIF1A",
            "entity_name": "KIF1A",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T13:27:29.349000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "edited their review of DST",
            "entity_name": "DST",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T13:27:08.595000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "edited their review of DST",
            "entity_name": "DST",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T13:26:23.527000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "edited their review of DST",
            "entity_name": "DST",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T12:47:41.145000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "added DST to panel",
            "entity_name": "DST",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T12:47:41.092000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "reviewed DST",
            "entity_name": "DST",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T12:40:23.953000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "edited their review of TECPR2",
            "entity_name": "TECPR2",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T12:22:28.979000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "added TECPR2 to panel",
            "entity_name": "TECPR2",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T12:22:28.938000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "reviewed TECPR2",
            "entity_name": "TECPR2",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T12:17:54.563000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "edited their review of NTRK1",
            "entity_name": "NTRK1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T12:15:21.313000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "commented on NTRK1",
            "entity_name": "NTRK1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T12:07:52.089000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "edited their review of NGF",
            "entity_name": "NGF",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:58:17.092000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "commented on NGF",
            "entity_name": "NGF",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:33:29.010000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on ADCK3",
            "entity_name": "ADCK3",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:32:29.840000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked ADCK3 as ready",
            "entity_name": "ADCK3",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:32:00.300000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified ADCK3 as green",
            "entity_name": "ADCK3",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:29:16.191000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "added ADCK3 to panel",
            "entity_name": "ADCK3",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:29:15.117000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "reviewed ADCK3",
            "entity_name": "ADCK3",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:20:17.085000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "edited their review of IKBKAP",
            "entity_name": "IKBKAP",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:20:06.680000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "edited their review of IKBKAP",
            "entity_name": "IKBKAP",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:07:53.381000Z",
            "panel_name": "Familial dysautonomia",
            "panel_id": 7,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "commented on IKBKAP",
            "entity_name": "IKBKAP",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:07:09.876000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified MPLKIP as amber",
            "entity_name": "MPLKIP",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:06:59.816000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "added MPLKIP to panel",
            "entity_name": "MPLKIP",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:06:58.750000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "reviewed MPLKIP",
            "entity_name": "MPLKIP",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:01:25.999000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified BCAP31 as amber",
            "entity_name": "BCAP31",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T11:01:25.999000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on BCAP31",
            "entity_name": "BCAP31",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T10:57:12.223000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified L2HGDH as amber",
            "entity_name": "L2HGDH",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T10:56:53.435000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "added L2HGDH to panel",
            "entity_name": "L2HGDH",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T10:56:52.405000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "reviewed L2HGDH",
            "entity_name": "L2HGDH",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T10:49:43.300000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified D2HGDH as amber",
            "entity_name": "D2HGDH",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T10:46:49.324000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "added D2HGDH to panel",
            "entity_name": "D2HGDH",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T10:46:48.163000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "reviewed D2HGDH",
            "entity_name": "D2HGDH",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T10:26:57.787000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified GJA1 as amber",
            "entity_name": "GJA1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T10:00:51.235000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "classified SDHD as red",
            "entity_name": "SDHD",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T10:00:28.545000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "classified SDHD as red",
            "entity_name": "SDHD",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:53:49.460000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on RARS",
            "entity_name": "RARS",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:53:49.460000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified RARS as amber",
            "entity_name": "RARS",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:44:01.853000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked PEX19 as ready",
            "entity_name": "PEX19",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:43:55.520000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified PEX19 as amber",
            "entity_name": "PEX19",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:43:13.500000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked PEX14 as ready",
            "entity_name": "PEX14",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:43:04.741000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified PEX14 as amber",
            "entity_name": "PEX14",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:37:55.943000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified MPZ as amber",
            "entity_name": "MPZ",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:37:55.943000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on MPZ",
            "entity_name": "MPZ",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:24:28.270000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified MEF2C as amber",
            "entity_name": "MEF2C",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:24:28.269000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on MEF2C",
            "entity_name": "MEF2C",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:14:24.970000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked COX15 as ready",
            "entity_name": "COX15",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:13:42.483000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified COX15 as green",
            "entity_name": "COX15",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:03:14.450000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on ARX",
            "entity_name": "ARX",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T09:03:14.450000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified ARX as amber",
            "entity_name": "ARX",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T08:58:27.469000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified AIMP1 as amber",
            "entity_name": "AIMP1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T08:07:31.061000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified AIMP1 as amber",
            "entity_name": "AIMP1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T08:07:31.061000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on AIMP1",
            "entity_name": "AIMP1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T07:45:35.699000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "added SDHD to panel",
            "entity_name": "SDHD",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T07:45:34.694000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Sarah Leigh",
            "item_type": "entity",
            "text": "reviewed SDHD",
            "entity_name": "SDHD",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T07:17:32.868000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked AARS2 as ready",
            "entity_name": "AARS2",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-26T07:17:06.632000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified AARS2 as green",
            "entity_name": "AARS2",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:26:44.541000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified MRPS16 as amber",
            "entity_name": "MRPS16",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:20:06.477000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified TUBA1A as amber",
            "entity_name": "TUBA1A",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:20:06.476000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on TUBA1A",
            "entity_name": "TUBA1A",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:16:04.345000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified RELN as amber",
            "entity_name": "RELN",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:15:58.106000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on RELN",
            "entity_name": "RELN",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:15:58.106000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified RELN as green",
            "entity_name": "RELN",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:11:46.671000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked PEX2 as ready",
            "entity_name": "PEX2",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:10:38.584000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified PAFAH1B1 as amber",
            "entity_name": "PAFAH1B1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:10:38.583000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on PAFAH1B1",
            "entity_name": "PAFAH1B1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:05:41.696000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified NDE1 as amber",
            "entity_name": "NDE1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:05:41.695000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on NDE1",
            "entity_name": "NDE1",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T15:02:28.688000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "marked HEPACAM as ready",
            "entity_name": "HEPACAM",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T14:53:56.039000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified FLVCR2 as amber",
            "entity_name": "FLVCR2",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T14:53:56.038000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on FLVCR2",
            "entity_name": "FLVCR2",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T14:44:50.018000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "classified DCX as amber",
            "entity_name": "DCX",
            "entity_type": "gene"
        },
        {
            "created": "2016-08-25T14:44:50.017000Z",
            "panel_name": "Inherited white matter disorders",
            "panel_id": 42,
            "panel_version": null,
            "user_name": "Ellen McDonagh",
            "item_type": "entity",
            "text": "commented on DCX",
            "entity_name": "DCX",
            "entity_type": "gene"
        }
    ]
}