{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2065","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2063","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"}]}