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{
"count": 220363,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2066",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2064",
"results": [
{
"created": "2019-12-06T18:53:39.147330+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.642",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALDOA as ready",
"entity_name": "ALDOA",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:53:39.140262+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.642",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aldoa has been classified as Amber List (Moderate Evidence).",
"entity_name": "ALDOA",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:53:32.937032+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.642",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ALDOA were changed from to Glycogen storage disease XII, MIM#611881",
"entity_name": "ALDOA",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:53:20.453957+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.641",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ALDOA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALDOA",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:53:05.812949+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.640",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ALDOA as Amber List (moderate evidence)",
"entity_name": "ALDOA",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:53:05.805634+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.640",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aldoa has been classified as Amber List (Moderate Evidence).",
"entity_name": "ALDOA",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:52:10.138059+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.639",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AKR1C2 as ready",
"entity_name": "AKR1C2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:52:10.130745+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.639",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: akr1c2 has been classified as Red List (Low Evidence).",
"entity_name": "AKR1C2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:52:03.847792+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.639",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AKR1C2 were changed from to 46XY sex reversal 8, MIM#614279",
"entity_name": "AKR1C2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:51:48.666785+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.638",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AKR1C2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AKR1C2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:51:32.436303+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.637",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AKR1C2 as Red List (low evidence)",
"entity_name": "AKR1C2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:51:32.428963+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.637",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: akr1c2 has been classified as Red List (Low Evidence).",
"entity_name": "AKR1C2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:50:03.876102+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.636",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AKAP6 as ready",
"entity_name": "AKAP6",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:50:03.868228+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.636",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: akap6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "AKAP6",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:48:26.826859+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.636",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AKAP6 were changed from to Intellectual disability",
"entity_name": "AKAP6",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:48:02.524840+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.635",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: AKAP6 were set to ",
"entity_name": "AKAP6",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:47:49.120858+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.634",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AKAP6 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "AKAP6",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:47:41.933038+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.633",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AKAP6 as Amber List (moderate evidence)",
"entity_name": "AKAP6",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:47:41.923981+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.633",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: akap6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "AKAP6",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:47:01.439075+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.632",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AGTR2 as ready",
"entity_name": "AGTR2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:47:01.431573+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.632",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: agtr2 has been classified as Red List (Low Evidence).",
"entity_name": "AGTR2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:46:54.737871+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.632",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AGTR2 as Red List (low evidence)",
"entity_name": "AGTR2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:46:54.731055+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.632",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: agtr2 has been classified as Red List (Low Evidence).",
"entity_name": "AGTR2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:46:07.990764+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.631",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AGT as ready",
"entity_name": "AGT",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:46:07.983407+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.631",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: agt has been classified as Red List (Low Evidence).",
"entity_name": "AGT",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:45:59.802553+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.631",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AGT were changed from to Renal tubular dysgenesis, MIM#267430",
"entity_name": "AGT",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:45:43.045272+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.630",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AGT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AGT",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:45:31.618531+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.629",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AGT as Red List (low evidence)",
"entity_name": "AGT",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:45:31.611338+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.629",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: agt has been classified as Red List (Low Evidence).",
"entity_name": "AGT",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:45:05.242408+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.628",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AGPS as ready",
"entity_name": "AGPS",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:45:05.234246+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.628",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: agps has been classified as Red List (Low Evidence).",
"entity_name": "AGPS",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:45:00.675438+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.628",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AGPS were changed from to Rhizomelic chondrodysplasia punctata, type 3, MIM#600121",
"entity_name": "AGPS",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:44:45.980501+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.627",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AGPS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AGPS",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:44:34.878097+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.626",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AGPS as Red List (low evidence)",
"entity_name": "AGPS",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:44:34.870861+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.626",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: agps has been classified as Red List (Low Evidence).",
"entity_name": "AGPS",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:44:03.758382+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.625",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AGK as ready",
"entity_name": "AGK",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:44:03.751283+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.625",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: agk has been classified as Red List (Low Evidence).",
"entity_name": "AGK",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:43:59.401823+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.625",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AGK were changed from to Sengers syndrome, MIM#212350",
"entity_name": "AGK",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:43:47.429986+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AGK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AGK",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:43:40.363692+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.623",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AGK as Red List (low evidence)",
"entity_name": "AGK",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:43:40.356817+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.623",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: agk has been classified as Red List (Low Evidence).",
"entity_name": "AGK",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:43:12.296311+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.622",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AGGF1 as ready",
"entity_name": "AGGF1",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:43:12.289272+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.622",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aggf1 has been classified as Red List (Low Evidence).",
"entity_name": "AGGF1",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:43:03.972678+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.622",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AGGF1 as Red List (low evidence)",
"entity_name": "AGGF1",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:43:03.965402+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.622",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aggf1 has been classified as Red List (Low Evidence).",
"entity_name": "AGGF1",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:42:35.094888+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.621",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AFG3L2 as ready",
"entity_name": "AFG3L2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:42:35.087671+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.621",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: afg3l2 has been classified as Red List (Low Evidence).",
"entity_name": "AFG3L2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:42:31.100369+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.621",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AFG3L2 were changed from to Spastic ataxia 5, autosomal recessive, MIM#614487",
"entity_name": "AFG3L2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:42:17.427955+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.620",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AFG3L2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AFG3L2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:42:05.334797+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.619",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AFG3L2 as Red List (low evidence)",
"entity_name": "AFG3L2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:42:05.327235+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.619",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: afg3l2 has been classified as Red List (Low Evidence).",
"entity_name": "AFG3L2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:41:19.576692+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.618",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHD1 as ready",
"entity_name": "CHD1",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:41:19.569743+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.618",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chd1 has been classified as Green List (High Evidence).",
"entity_name": "CHD1",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:41:13.545611+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.618",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CHD1 as Green List (high evidence)",
"entity_name": "CHD1",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:41:13.536691+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.618",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chd1 has been classified as Green List (High Evidence).",
"entity_name": "CHD1",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:39:45.277515+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.617",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADCY5 as ready",
"entity_name": "ADCY5",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:39:45.270486+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.617",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adcy5 has been classified as Red List (Low Evidence).",
"entity_name": "ADCY5",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:39:39.948620+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.617",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADCY5 were changed from to Dyskinesia, familial, with facial myokymia, MIM#606703",
"entity_name": "ADCY5",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:39:24.787801+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.616",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ADCY5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ADCY5",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:39:13.699720+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.615",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ADCY5 as Red List (low evidence)",
"entity_name": "ADCY5",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:39:13.692777+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.615",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adcy5 has been classified as Red List (Low Evidence).",
"entity_name": "ADCY5",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:38:32.551975+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.614",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADAMTSL2 as ready",
"entity_name": "ADAMTSL2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:38:32.544560+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.614",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adamtsl2 has been classified as Red List (Low Evidence).",
"entity_name": "ADAMTSL2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:38:25.855831+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.614",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADAMTSL2 were changed from to Geleophysic dysplasia 1, MIM#231050",
"entity_name": "ADAMTSL2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:38:09.440893+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ADAMTSL2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADAMTSL2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:37:58.632574+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.612",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ADAMTSL2 as Red List (low evidence)",
"entity_name": "ADAMTSL2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:37:58.618142+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.612",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adamtsl2 has been classified as Red List (Low Evidence).",
"entity_name": "ADAMTSL2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:36:31.152080+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.611",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADA2 as ready",
"entity_name": "ADA2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:36:31.144767+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.611",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ada2 has been classified as Red List (Low Evidence).",
"entity_name": "ADA2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:36:26.773232+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.611",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADA2 were changed from to Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome, MIM#615688",
"entity_name": "ADA2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:35:54.577984+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.610",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ADA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADA2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:35:43.628667+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.609",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ADA2 as Red List (low evidence)",
"entity_name": "ADA2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:35:43.621190+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.609",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ada2 has been classified as Red List (Low Evidence).",
"entity_name": "ADA2",
"entity_type": "gene"
},
{
"created": "2019-12-06T15:24:40.378973+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MIR17HG as ready",
"entity_name": "MIR17HG",
"entity_type": "gene"
},
{
"created": "2019-12-06T15:24:40.370970+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mir17hg has been classified as Green List (High Evidence).",
"entity_name": "MIR17HG",
"entity_type": "gene"
},
{
"created": "2019-12-06T15:24:31.337730+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MIR17HG as Green List (high evidence)",
"entity_name": "MIR17HG",
"entity_type": "gene"
},
{
"created": "2019-12-06T15:24:31.330200+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mir17hg has been classified as Green List (High Evidence).",
"entity_name": "MIR17HG",
"entity_type": "gene"
},
{
"created": "2019-12-06T15:24:11.020818+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.167",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MIR17HG was added\ngene: MIR17HG was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: MIR17HG was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: MIR17HG were set to 25391829; 21892160\nPhenotypes for gene: MIR17HG were set to Feingold syndrome 2; OMIM #614326\nReview for gene: MIR17HG was set to GREEN\nAdded comment: 4 unrelated cases reported - 3 with gene deletions, 1 with SNV \nSources: Expert list",
"entity_name": "MIR17HG",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:56:43.891512+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.608",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MAP4K4 as ready",
"entity_name": "MAP4K4",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:56:43.884377+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.608",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: map4k4 has been classified as Red List (Low Evidence).",
"entity_name": "MAP4K4",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:56:31.558155+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.608",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MAP4K4 was added\ngene: MAP4K4 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list\nMode of inheritance for gene: MAP4K4 was set to Unknown\nReview for gene: MAP4K4 was set to RED\nAdded comment: Cannot find evidence for gene-disease association. \nSources: Expert list",
"entity_name": "MAP4K4",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:44:36.499037+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.607",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LZTR1 as ready",
"entity_name": "LZTR1",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:44:36.491830+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.607",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lztr1 has been classified as Green List (High Evidence).",
"entity_name": "LZTR1",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:44:30.929789+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.607",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: LZTR1 as Green List (high evidence)",
"entity_name": "LZTR1",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:44:30.922645+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.607",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lztr1 has been classified as Green List (High Evidence).",
"entity_name": "LZTR1",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:44:18.415894+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.606",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LZTR1 was added\ngene: LZTR1 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list\nMode of inheritance for gene: LZTR1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: LZTR1 were set to Noonan syndrome 10, MIM#616564; Noonan syndrome 2, MIM#605275\nReview for gene: LZTR1 was set to GREEN\nAdded comment: Sources: Expert list",
"entity_name": "LZTR1",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:39:36.162509+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.605",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAMB2 as ready",
"entity_name": "LAMB2",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:39:36.153997+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.605",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lamb2 has been classified as Green List (High Evidence).",
"entity_name": "LAMB2",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:39:30.924284+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.605",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LAMB2 were changed from to Pierson syndrome, MIM#609049",
"entity_name": "LAMB2",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:38:56.138864+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.604",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LAMB2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAMB2",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:38:22.659774+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.603",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LAMB2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pierson syndrome, MIM#609049; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAMB2",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:19:36.523195+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.603",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LZTFL1 as ready",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:19:36.515817+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.603",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lztfl1 has been classified as Green List (High Evidence).",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:19:32.879039+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.603",
"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": "2019-12-06T14:19:19.850326+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.602",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LZTFL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22510444, 23692385, 27312011; Phenotypes: Bardet-Biedl syndrome 17, MIM#615994; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LZTFL1",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:13:46.721706+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.602",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LYST as ready",
"entity_name": "LYST",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:13:46.714706+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.602",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lyst has been classified as Green List (High Evidence).",
"entity_name": "LYST",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:13:42.594012+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.602",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LYST were changed from to Chediak-Higashi syndrome, MIM#214500",
"entity_name": "LYST",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:13:28.701415+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.601",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LYST was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LYST",
"entity_type": "gene"
},
{
"created": "2019-12-06T14:13:14.846010+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.600",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LYST: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Chediak-Higashi syndrome, MIM#214500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LYST",
"entity_type": "gene"
}
]
}