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{
"count": 220363,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2065",
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"results": [
{
"created": "2019-12-06T19:52:33.927477+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.694",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: add3 has been classified as Green List (High Evidence).",
"entity_name": "ADD3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:52:28.292903+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.694",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADD3 were changed from to Cerebral palsy, spastic quadriplegic, 3, MIM#617008",
"entity_name": "ADD3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:52:14.050788+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.693",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ADD3 were set to ",
"entity_name": "ADD3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:52:01.041628+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.692",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ADD3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADD3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:51:13.579157+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.691",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADAT3 as ready",
"entity_name": "ADAT3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:51:13.571774+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.691",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adat3 has been classified as Green List (High Evidence).",
"entity_name": "ADAT3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:51:08.663888+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.691",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADAT3 were changed from to Mental retardation, autosomal recessive 36, MIM#615286",
"entity_name": "ADAT3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:50:53.963813+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.690",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ADAT3 were set to ",
"entity_name": "ADAT3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:50:41.939829+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.689",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ADAT3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADAT3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:49:59.044060+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.688",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADAMTS10 as ready",
"entity_name": "ADAMTS10",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:49:59.036588+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.688",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adamts10 has been classified as Green List (High Evidence).",
"entity_name": "ADAMTS10",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:49:53.930021+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.688",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADAMTS10 were changed from to Weill-Marchesani syndrome 1, recessive, MIM#277600",
"entity_name": "ADAMTS10",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:49:39.629337+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.687",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ADAMTS10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADAMTS10",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:48:47.478377+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.686",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ACTL6A as ready",
"entity_name": "ACTL6A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:48:47.466270+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.686",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: actl6a has been classified as Green List (High Evidence).",
"entity_name": "ACTL6A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:48:43.095608+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.686",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ACTL6A were changed from to Intellectual disability",
"entity_name": "ACTL6A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:48:31.208283+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.685",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ACTL6A were set to ",
"entity_name": "ACTL6A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:48:21.940823+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ACTL6A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ACTL6A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:46:57.846438+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.683",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AVPR2 as ready",
"entity_name": "AVPR2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:46:57.839289+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.683",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: avpr2 has been classified as Red List (Low Evidence).",
"entity_name": "AVPR2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:46:52.148734+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.683",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AVPR2 were changed from to Diabetes insipidus, nephrogenic, MIM#304800",
"entity_name": "AVPR2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:46:30.762595+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AVPR2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "AVPR2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:46:18.876536+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.681",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AVPR2 as Red List (low evidence)",
"entity_name": "AVPR2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:46:18.868916+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.681",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: avpr2 has been classified as Red List (Low Evidence).",
"entity_name": "AVPR2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:45:28.965919+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AVPR1A as ready",
"entity_name": "AVPR1A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:45:28.958952+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: avpr1a has been classified as Red List (Low Evidence).",
"entity_name": "AVPR1A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:45:22.649188+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AVPR1A as Red List (low evidence)",
"entity_name": "AVPR1A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:45:22.641605+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: avpr1a has been classified as Red List (Low Evidence).",
"entity_name": "AVPR1A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:44:52.898931+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.679",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AVP as ready",
"entity_name": "AVP",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:44:52.891251+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.679",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: avp has been classified as Red List (Low Evidence).",
"entity_name": "AVP",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:44:47.497499+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.679",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AVP were changed from to Diabetes insipidus, neurohypophyseal, MIM#125700",
"entity_name": "AVP",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:44:37.297513+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.678",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AVP was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "AVP",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:44:18.600307+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AVP as Red List (low evidence)",
"entity_name": "AVP",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:44:18.592932+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: avp has been classified as Red List (Low Evidence).",
"entity_name": "AVP",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:42:20.822073+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.676",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATXN10 as ready",
"entity_name": "ATXN10",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:42:20.814612+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.676",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atxn10 has been classified as Red List (Low Evidence).",
"entity_name": "ATXN10",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:42:15.847275+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.676",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ATXN10 were changed from to Spinocerebellar ataxia 10, MIM#603516",
"entity_name": "ATXN10",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:42:00.235444+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.675",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ATXN10 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ATXN10",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:41:52.920195+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.674",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATXN10 as Red List (low evidence)",
"entity_name": "ATXN10",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:41:52.910739+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.674",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atxn10 has been classified as Red List (Low Evidence).",
"entity_name": "ATXN10",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:07:04.093207+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATP8A2 as ready",
"entity_name": "ATP8A2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:07:04.086150+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp8a2 has been classified as Green List (High Evidence).",
"entity_name": "ATP8A2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:06:59.721694+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ATP8A2 were changed from to Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4, MIM#615268",
"entity_name": "ATP8A2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:06:50.050844+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ATP8A2 were set to ",
"entity_name": "ATP8A2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:06:37.437023+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ATP8A2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ATP8A2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:04:58.764115+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATP2B3 as ready",
"entity_name": "ATP2B3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:04:58.756412+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp2b3 has been classified as Red List (Low Evidence).",
"entity_name": "ATP2B3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:04:53.571905+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ATP2B3 were changed from to Spinocerebellar ataxia, X-linked 1, MIM#302500",
"entity_name": "ATP2B3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:04:45.706560+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ATP2B3 were set to ",
"entity_name": "ATP2B3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:04:32.584019+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATP2B3 as Red List (low evidence)",
"entity_name": "ATP2B3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:04:32.576648+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp2b3 has been classified as Red List (Low Evidence).",
"entity_name": "ATP2B3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:03:29.191665+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATP2A2 as ready",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:03:29.184005+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp2a2 has been classified as Red List (Low Evidence).",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:03:23.404567+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ATP2A2 were changed from to Darier disease, MIM#124200",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:03:15.188106+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ATP2A2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:02:55.802456+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.665",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATP2A2 as Red List (low evidence)",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:02:55.793718+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.665",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp2a2 has been classified as Red List (Low Evidence).",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:01:59.275800+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATP1A3 as ready",
"entity_name": "ATP1A3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:01:59.268766+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp1a3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ATP1A3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:01:37.547430+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ATP1A3 were changed from to Alternating hemiplegia of childhood 2, MIM#614820",
"entity_name": "ATP1A3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:01:33.249114+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.663",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ATP1A3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ATP1A3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:00:49.989087+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATP1A3 as Amber List (moderate evidence)",
"entity_name": "ATP1A3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:00:49.981723+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp1a3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ATP1A3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:00:17.473428+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.661",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATP10A as ready",
"entity_name": "ATP10A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:00:17.466261+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.661",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp10a has been classified as Red List (Low Evidence).",
"entity_name": "ATP10A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:00:12.967505+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.661",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ATP10A were set to ",
"entity_name": "ATP10A",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:00:04.498410+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.660",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ATP10A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ATP10A",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:59:52.162271+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.659",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATP10A as Red List (low evidence)",
"entity_name": "ATP10A",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:59:52.152969+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.659",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp10a has been classified as Red List (Low Evidence).",
"entity_name": "ATP10A",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:59:18.974961+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ARNT2 as ready",
"entity_name": "ARNT2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:59:18.967558+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arnt2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ARNT2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:59:13.812396+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ARNT2 were changed from to Webb-Dattani syndrome 615926",
"entity_name": "ARNT2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:59:01.117549+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.657",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ARNT2 were set to ",
"entity_name": "ARNT2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:58:52.762029+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ARNT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ARNT2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:58:45.298088+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.655",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ARNT2 as Amber List (moderate evidence)",
"entity_name": "ARNT2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:58:45.290895+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.655",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arnt2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ARNT2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:58:03.897270+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.654",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ARHGAP31 as ready",
"entity_name": "ARHGAP31",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:58:03.890169+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.654",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arhgap31 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ARHGAP31",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:57:58.786924+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.654",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ARHGAP31 were changed from to Adams-Oliver syndrome 1, MIM#100300",
"entity_name": "ARHGAP31",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:57:45.770391+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.653",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ARHGAP31 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ARHGAP31",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:57:34.264399+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.652",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ARHGAP31 as Amber List (moderate evidence)",
"entity_name": "ARHGAP31",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:57:34.257294+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.652",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arhgap31 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ARHGAP31",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:57:03.155012+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.651",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: APTX as ready",
"entity_name": "APTX",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:57:03.147612+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.651",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aptx has been classified as Red List (Low Evidence).",
"entity_name": "APTX",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:56:58.834512+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.651",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: APTX were changed from to Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia, MIM#208920",
"entity_name": "APTX",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:56:50.366647+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.650",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: APTX was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "APTX",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:56:31.166869+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.649",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: APTX as Red List (low evidence)",
"entity_name": "APTX",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:56:31.158305+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.649",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aptx has been classified as Red List (Low Evidence).",
"entity_name": "APTX",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:55:53.181230+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.648",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ANKH as ready",
"entity_name": "ANKH",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:55:53.174095+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.648",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ankh has been classified as Red List (Low Evidence).",
"entity_name": "ANKH",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:55:46.610715+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.648",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ANKH were changed from to Craniometaphyseal dysplasia, MIM#123000",
"entity_name": "ANKH",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:55:33.211988+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.647",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ANKH was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ANKH",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:55:24.647973+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.646",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ANKH as Red List (low evidence)",
"entity_name": "ANKH",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:55:24.635631+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.646",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ankh has been classified as Red List (Low Evidence).",
"entity_name": "ANKH",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:54:51.704543+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.645",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALS2 as ready",
"entity_name": "ALS2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:54:51.696248+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.645",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: als2 has been classified as Red List (Low Evidence).",
"entity_name": "ALS2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:54:44.392194+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.645",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ALS2 were changed from to Spastic paralysis, infantile onset ascending, MIM#607225",
"entity_name": "ALS2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:54:34.949385+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.644",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ALS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALS2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:54:20.172360+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.643",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ALS2 as Red List (low evidence)",
"entity_name": "ALS2",
"entity_type": "gene"
},
{
"created": "2019-12-06T18:54:20.165489+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.643",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: als2 has been classified as Red List (Low Evidence).",
"entity_name": "ALS2",
"entity_type": "gene"
}
]
}