GET /api/v1/activities/?format=api&page=1720
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{
    "count": 221304,
    "next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1721",
    "previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1719",
    "results": [
        {
            "created": "2020-07-22T06:57:48.670997+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.147",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "reviewed gene: TWIST1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Robinow-Sorauf syndrome, MIM# 180750; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "TWIST1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-22T00:03:29.114979+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.147",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TWIST1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "TWIST1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-22T00:02:56.331637+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.146",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TTC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "TTC8",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-22T00:02:27.109463+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.145",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TTC21B was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "entity_name": "TTC21B",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-22T00:01:56.853388+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.144",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TRAF3IP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "TRAF3IP1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-22T00:01:18.616741+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.143",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TMEM67 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "TMEM67",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-22T00:00:44.387452+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.142",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TMEM237 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "TMEM237",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-22T00:00:12.865250+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.141",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TMEM231 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "TMEM231",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:59:40.633345+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.140",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TMEM216 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "TMEM216",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:59:10.787994+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.139",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TMEM138 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "TMEM138",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:58:39.052059+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.138",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TFAP2B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "TFAP2B",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:58:10.534130+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.137",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TFAP2A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "TFAP2A",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:57:41.757615+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.136",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TCTN3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "TCTN3",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:57:12.647281+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.135",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TCTN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "TCTN2",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:56:44.231210+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.134",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TCTEX1D2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "TCTEX1D2",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:56:15.756962+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.133",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TBX5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "TBX5",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:55:39.657437+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.132",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TBX3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "TBX3",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:55:10.744888+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.131",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: TBX22 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
            "entity_name": "TBX22",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:54:39.222196+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.130",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: SPINT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "SPINT2",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:54:08.497896+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.129",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: SMOC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "SMOC1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:53:01.457208+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.128",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: SHH was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "SHH",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:48:15.088427+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.127",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: SDCCAG8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "SDCCAG8",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:47:39.897364+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.126",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: SC5D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "SC5D",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:47:11.435242+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.125",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: SALL4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "SALL4",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:46:42.317976+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.124",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: SALL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "SALL1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:39:30.630447+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.123",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: RPGRIP1L was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "RPGRIP1L",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:38:49.889949+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.122",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: RBM10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "RBM10",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:38:21.248050+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.121",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: RAB23 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "RAB23",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:37:36.640129+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.120",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Marked gene: PROM1 as ready",
            "entity_name": "PROM1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:37:36.632661+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.120",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Gene: prom1 has been classified as Red List (Low Evidence).",
            "entity_name": "PROM1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:37:32.108202+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.120",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Phenotypes for gene: PROM1 were changed from  to Cone-rod dystrophy 12, MIM# 612657; Macular dystrophy, retinal, 2, MIM# 608051; Retinitis pigmentosa 41, MIM# 612095; Stargardt disease 4, MIM# 603786",
            "entity_name": "PROM1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:37:02.675415+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.119",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Classified gene: PROM1 as Red List (low evidence)",
            "entity_name": "PROM1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:37:02.662440+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.119",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Gene: prom1 has been classified as Red List (Low Evidence).",
            "entity_name": "PROM1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:36:38.012393+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.118",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "reviewed gene: PROM1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Cone-rod dystrophy 12, MIM# 612657, Macular dystrophy, retinal, 2, MIM# 608051, Retinitis pigmentosa 41, MIM# 612095, Stargardt disease 4, MIM# 603786; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "entity_name": "PROM1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:33:21.824558+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.118",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: PROM1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "entity_name": "PROM1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:32:50.303827+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.117",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: PORCN was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
            "entity_name": "PORCN",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:32:17.072577+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.116",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: PNPLA6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "PNPLA6",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:31:45.509457+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.115",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: PITX1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "PITX1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:31:05.750009+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.114",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: PIK3R2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "PIK3R2",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:30:36.833981+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.113",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Marked gene: PIK3CA as ready",
            "entity_name": "PIK3CA",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:30:36.829388+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.113",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Added comment: Comment when marking as ready: Germline variants also described.",
            "entity_name": "PIK3CA",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:30:36.794888+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.113",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Gene: pik3ca has been classified as Green List (High Evidence).",
            "entity_name": "PIK3CA",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:30:33.699274+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.113",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Phenotypes for gene: PIK3CA were changed from  to Megalencephaly-capillary malformation (MCAP) syndrome , MIM#602501",
            "entity_name": "PIK3CA",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:28:34.928018+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.112",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: PIK3CA was changed from Unknown to Other",
            "entity_name": "PIK3CA",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:28:05.570306+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.111",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Tag somatic tag was added to gene: PIK3CA.",
            "entity_name": "PIK3CA",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:27:41.608729+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.111",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: OFD1 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
            "entity_name": "OFD1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:27:11.005675+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.110",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: NPHP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "NPHP3",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:26:42.950564+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.109",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: NEK1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "NEK1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:26:14.769341+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.108",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: MKS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "MKS1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:25:46.491276+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.107",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: MKKS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "MKKS",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:25:19.214008+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.106",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: MEGF8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "MEGF8",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:24:49.218950+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.105",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: MBTPS2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "entity_name": "MBTPS2",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:24:20.592340+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.104",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: LZTFL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "LZTFL1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:23:36.376392+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.103",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "edited their review of gene: LRP4: Changed phenotypes: Cenani-Lenz syndactyly syndrome, MIM# 212780, Sclerosteosis 2, MIM# 614305",
            "entity_name": "LRP4",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:23:26.598744+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.103",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Marked gene: LRP4 as ready",
            "entity_name": "LRP4",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:23:26.591670+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.103",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Gene: lrp4 has been classified as Red List (Low Evidence).",
            "entity_name": "LRP4",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:23:16.337700+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.103",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "edited their review of gene: LRP4: Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "entity_name": "LRP4",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:23:05.387774+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.103",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "reviewed gene: LRP4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
            "entity_name": "LRP4",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:22:44.098169+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.103",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Classified gene: LRP4 as Red List (low evidence)",
            "entity_name": "LRP4",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:22:44.091785+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.103",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Gene: lrp4 has been classified as Red List (Low Evidence).",
            "entity_name": "LRP4",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:22:26.639877+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.102",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: LRP4 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "entity_name": "LRP4",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:22:09.352168+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.101",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Phenotypes for gene: LRP4 were changed from  to Cenani-Lenz syndactyly syndrome, MIM#\t212780; Sclerosteosis 2, MIM#\t614305",
            "entity_name": "LRP4",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:19:34.789734+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.100",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Phenotypes for gene: LMBR1 were changed from  to Polydactyly, preaxial type II, MIM#\t174500",
            "entity_name": "LMBR1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:19:18.152430+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.99",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: LMBR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "LMBR1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:18:06.101992+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.98",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Marked gene: LBR as ready",
            "entity_name": "LBR",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:18:06.091617+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.98",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Gene: lbr has been classified as Green List (High Evidence).",
            "entity_name": "LBR",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:18:01.508835+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.98",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Phenotypes for gene: LBR were changed from  to Greenberg skeletal dysplasia, MIM#\t215140",
            "entity_name": "LBR",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:17:35.469404+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.97",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: LBR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "LBR",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:16:31.635034+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.96",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: KIF7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "KIF7",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:16:04.548160+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.95",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: KIAA0586 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "KIAA0586",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:15:23.745163+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.94",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: INPP5E was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "INPP5E",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:14:57.892770+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.93",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: IFT80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "IFT80",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:14:23.908138+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.92",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: IFT52 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "IFT52",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:13:52.813772+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.91",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: IFT43 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "IFT43",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:13:25.931605+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.90",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: IFT27 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "IFT27",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:12:59.545305+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.89",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: IFT172 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "IFT172",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:12:32.686126+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.88",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: IFT140 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "IFT140",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:11:58.931690+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.87",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: ICK was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "entity_name": "ICK",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:11:18.696404+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.86",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: HYLS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "HYLS1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:10:53.299364+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.85",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Phenotypes for gene: HOXD13 were changed from  to Synpolydactyly 1, MIM#\t186000",
            "entity_name": "HOXD13",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:10:30.276638+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.84",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: HOXD13 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "HOXD13",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:09:44.347288+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.83",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: HOXA13 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "HOXA13",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:09:17.603614+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.82",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: HNRNPK was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "HNRNPK",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:08:47.346515+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.81",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: GRIP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "GRIP1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:08:18.720895+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.80",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: GPC3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "entity_name": "GPC3",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:07:47.207515+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.79",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: GLI3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "GLI3",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:07:23.112115+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.78",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: GLI2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "GLI2",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:06:53.960848+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.77",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: GDF5 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "entity_name": "GDF5",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:06:25.430339+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.76",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: FREM2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "FREM2",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:05:59.815070+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.75",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: FRAS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "FRAS1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:05:34.656089+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.74",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: FGFR3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "FGFR3",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:05:08.450304+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.73",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: FGFR2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "FGFR2",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:04:43.725203+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.72",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: FGFR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "FGFR1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:04:17.242201+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.71",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: FGF10 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "entity_name": "FGF10",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:03:51.040218+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.70",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: EVC2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "entity_name": "EVC2",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:03:25.435790+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.69",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: EVC was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
            "entity_name": "EVC",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:02:33.963874+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.68",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: EVC was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "EVC",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:01:46.790517+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.67",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: EBP was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
            "entity_name": "EBP",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:01:19.687269+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.66",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: DYNC2LI1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "DYNC2LI1",
            "entity_type": "gene"
        },
        {
            "created": "2020-07-21T23:00:55.125030+10:00",
            "panel_name": "Polydactyly",
            "panel_id": 159,
            "panel_version": "0.65",
            "user_name": "Zornitza Stark",
            "item_type": "entity",
            "text": "Mode of inheritance for gene: DYNC2H1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
            "entity_name": "DYNC2H1",
            "entity_type": "gene"
        }
    ]
}