{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2063","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2061","results":[{"created":"2019-12-07T11:38:16.693639+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.794","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cfhr1 has been classified as Red List (Low Evidence).","entity_name":"CFHR1","entity_type":"gene"},{"created":"2019-12-07T11:38:12.374495+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.794","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CFHR1 were changed from  to Hemolytic uremic syndrome, atypical, susceptibility to, MIM#235400","entity_name":"CFHR1","entity_type":"gene"},{"created":"2019-12-07T11:37:52.593646+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.793","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CFHR1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CFHR1","entity_type":"gene"},{"created":"2019-12-07T11:37:43.706867+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.792","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CFHR1 as Red List (low evidence)","entity_name":"CFHR1","entity_type":"gene"},{"created":"2019-12-07T11:37:43.699356+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.792","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cfhr1 has been classified as Red List (Low Evidence).","entity_name":"CFHR1","entity_type":"gene"},{"created":"2019-12-07T11:37:06.208273+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.791","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CFH as ready","entity_name":"CFH","entity_type":"gene"},{"created":"2019-12-07T11:37:06.201216+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.791","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cfh has been classified as Red List (Low Evidence).","entity_name":"CFH","entity_type":"gene"},{"created":"2019-12-07T11:37:01.776346+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.791","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CFH were changed from  to Complement factor H deficiency, MIM#609814","entity_name":"CFH","entity_type":"gene"},{"created":"2019-12-07T11:36:49.017165+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.790","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CFH was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CFH","entity_type":"gene"},{"created":"2019-12-07T11:36:37.785124+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.789","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CFH as Red List (low evidence)","entity_name":"CFH","entity_type":"gene"},{"created":"2019-12-07T11:36:37.777608+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.789","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cfh has been classified as Red List (Low Evidence).","entity_name":"CFH","entity_type":"gene"},{"created":"2019-12-07T11:36:05.969878+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.788","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP89 as ready","entity_name":"CEP89","entity_type":"gene"},{"created":"2019-12-07T11:36:05.962421+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.788","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep89 has been classified as Amber List (Moderate Evidence).","entity_name":"CEP89","entity_type":"gene"},{"created":"2019-12-07T11:36:01.421339+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.788","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CEP89 were changed from  to Mitochondrial complex IV deficiency","entity_name":"CEP89","entity_type":"gene"},{"created":"2019-12-07T11:35:40.872860+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.787","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CEP89 were set to ","entity_name":"CEP89","entity_type":"gene"},{"created":"2019-12-07T11:35:30.987239+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.786","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CEP89 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP89","entity_type":"gene"},{"created":"2019-12-07T11:35:24.483374+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.785","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CEP89 as Amber List (moderate evidence)","entity_name":"CEP89","entity_type":"gene"},{"created":"2019-12-07T11:35:24.475340+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.785","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep89 has been classified as Amber List (Moderate Evidence).","entity_name":"CEP89","entity_type":"gene"},{"created":"2019-12-07T11:34:25.069666+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.784","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP63 as ready","entity_name":"CEP63","entity_type":"gene"},{"created":"2019-12-07T11:34:25.062057+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.784","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep63 has been classified as Amber List (Moderate Evidence).","entity_name":"CEP63","entity_type":"gene"},{"created":"2019-12-07T11:34:19.627571+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.784","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CEP63 were changed from  to Seckel syndrome 6, MIM#614728","entity_name":"CEP63","entity_type":"gene"},{"created":"2019-12-07T11:34:06.772588+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.783","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CEP63 were set to ","entity_name":"CEP63","entity_type":"gene"},{"created":"2019-12-07T11:33:52.872871+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.782","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CEP63 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP63","entity_type":"gene"},{"created":"2019-12-07T11:33:45.679645+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.781","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CEP63 as Amber List (moderate evidence)","entity_name":"CEP63","entity_type":"gene"},{"created":"2019-12-07T11:33:45.669559+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.781","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep63 has been classified as Amber List (Moderate Evidence).","entity_name":"CEP63","entity_type":"gene"},{"created":"2019-12-07T09:57:32.707463+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.172","user_name":"Seb L","item_type":"entity","text":"Marked gene: WDR91 as ready","entity_name":"WDR91","entity_type":"gene"},{"created":"2019-12-07T09:57:32.698654+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.172","user_name":"Seb L","item_type":"entity","text":"Gene: wdr91 has been classified as Red List (Low Evidence).","entity_name":"WDR91","entity_type":"gene"},{"created":"2019-12-07T09:56:21.996543+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.172","user_name":"Seb L","item_type":"entity","text":"Classified gene: WDR91 as Red List (low evidence)","entity_name":"WDR91","entity_type":"gene"},{"created":"2019-12-07T09:56:21.989042+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.172","user_name":"Seb L","item_type":"entity","text":"Gene: wdr91 has been classified as Red List (Low Evidence).","entity_name":"WDR91","entity_type":"gene"},{"created":"2019-12-07T09:52:14.025219+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.2","user_name":"Seb L","item_type":"entity","text":"Classified gene: WDR91 as Red List (low evidence)","entity_name":"WDR91","entity_type":"gene"},{"created":"2019-12-07T09:52:14.010808+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.2","user_name":"Seb L","item_type":"entity","text":"Gene: wdr91 has been classified as Red List (Low Evidence).","entity_name":"WDR91","entity_type":"gene"},{"created":"2019-12-07T09:51:40.295310+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.1","user_name":"Seb L","item_type":"entity","text":"Marked gene: WDR91 as ready","entity_name":"WDR91","entity_type":"gene"},{"created":"2019-12-07T09:51:40.286597+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.1","user_name":"Seb L","item_type":"entity","text":"Gene: wdr91 has been classified as Green List (High Evidence).","entity_name":"WDR91","entity_type":"gene"},{"created":"2019-12-07T09:51:19.560316+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.1","user_name":"Seb L","item_type":"entity","text":"reviewed gene: WDR91: Rating: RED; Mode of pathogenicity: None; Publications: 28969387; Phenotypes: ; Mode of inheritance: Unknown","entity_name":"WDR91","entity_type":"gene"},{"created":"2019-12-07T07:23:46.821065+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.780","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CDT1 as ready","entity_name":"CDT1","entity_type":"gene"},{"created":"2019-12-07T07:23:46.813743+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.780","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdt1 has been classified as Red List (Low Evidence).","entity_name":"CDT1","entity_type":"gene"},{"created":"2019-12-07T07:23:41.936988+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.780","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CDT1 were changed from  to Meier-Gorlin syndrome 4, MIM#613804","entity_name":"CDT1","entity_type":"gene"},{"created":"2019-12-07T07:23:28.995329+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.779","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CDT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CDT1","entity_type":"gene"},{"created":"2019-12-07T07:23:21.362126+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.778","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CDT1 as Red List (low evidence)","entity_name":"CDT1","entity_type":"gene"},{"created":"2019-12-07T07:23:21.355371+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.778","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdt1 has been classified as Red List (Low Evidence).","entity_name":"CDT1","entity_type":"gene"},{"created":"2019-12-07T07:22:38.072711+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.777","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CDK6 as ready","entity_name":"CDK6","entity_type":"gene"},{"created":"2019-12-07T07:22:38.065822+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.777","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdk6 has been classified as Amber List (Moderate Evidence).","entity_name":"CDK6","entity_type":"gene"},{"created":"2019-12-07T07:22:32.711017+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.777","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CDK6 were changed from  to Microcephaly 12, primary, autosomal recessive, MIM#616080","entity_name":"CDK6","entity_type":"gene"},{"created":"2019-12-07T07:22:16.866206+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.776","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CDK6 were set to ","entity_name":"CDK6","entity_type":"gene"},{"created":"2019-12-07T07:22:01.788370+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.775","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CDK6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CDK6","entity_type":"gene"},{"created":"2019-12-07T07:21:49.567581+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.774","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CDK6 as Amber List (moderate evidence)","entity_name":"CDK6","entity_type":"gene"},{"created":"2019-12-07T07:21:49.560402+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.774","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdk6 has been classified as Amber List (Moderate Evidence).","entity_name":"CDK6","entity_type":"gene"},{"created":"2019-12-07T07:21:04.009568+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CDK16 as ready","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:21:04.000316+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdk16 has been classified as Amber List (Moderate Evidence).","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:20:54.253315+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CDK16 as Amber List (moderate evidence)","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:20:54.245714+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdk16 has been classified as Amber List (Moderate Evidence).","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:20:33.920603+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CDK16 was added\ngene: CDK16 was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: CDK16 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: CDK16 were set to 25644381\nPhenotypes for gene: CDK16 were set to Intellectual disability\nReview for gene: CDK16 was set to AMBER\nAdded comment: Single family described in this manuscript describing multiple candidate genes for XLID. \nSources: Expert list","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:16:15.191243+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.773","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CDK16 as ready","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:16:15.184051+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.773","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdk16 has been classified as Amber List (Moderate Evidence).","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:16:10.483152+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.773","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CDK16 were changed from  to Intellectual disability","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:15:52.818008+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.772","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CDK16 were set to ","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:15:39.156117+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.771","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CDK16 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:15:25.474642+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.770","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CDK16 as Amber List (moderate evidence)","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:15:25.465160+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.770","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdk16 has been classified as Amber List (Moderate Evidence).","entity_name":"CDK16","entity_type":"gene"},{"created":"2019-12-07T07:14:48.943935+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.769","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CD96 as ready","entity_name":"CD96","entity_type":"gene"},{"created":"2019-12-07T07:14:48.936416+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.769","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd96 has been classified as Amber List (Moderate Evidence).","entity_name":"CD96","entity_type":"gene"},{"created":"2019-12-07T07:14:44.547347+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.769","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CD96 were changed from  to C syndrome, MIM#211750","entity_name":"CD96","entity_type":"gene"},{"created":"2019-12-07T07:14:32.122259+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.768","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CD96 were set to ","entity_name":"CD96","entity_type":"gene"},{"created":"2019-12-07T07:14:19.904823+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.767","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CD96 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CD96","entity_type":"gene"},{"created":"2019-12-07T07:14:07.161391+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.766","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CD96 as Amber List (moderate evidence)","entity_name":"CD96","entity_type":"gene"},{"created":"2019-12-07T07:14:07.153089+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.766","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd96 has been classified as Amber List (Moderate Evidence).","entity_name":"CD96","entity_type":"gene"},{"created":"2019-12-06T21:38:31.404359+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.765","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CCDC8 as ready","entity_name":"CCDC8","entity_type":"gene"},{"created":"2019-12-06T21:38:31.397054+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.765","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc8 has been classified as Red List (Low Evidence).","entity_name":"CCDC8","entity_type":"gene"},{"created":"2019-12-06T21:38:26.709004+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.765","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CCDC8 were changed from  to 3-M syndrome 3, MIM#614205","entity_name":"CCDC8","entity_type":"gene"},{"created":"2019-12-06T21:38:17.893727+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.764","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CCDC8 were set to ","entity_name":"CCDC8","entity_type":"gene"},{"created":"2019-12-06T21:38:08.892032+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.763","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CCDC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CCDC8","entity_type":"gene"},{"created":"2019-12-06T21:37:58.117201+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.762","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CCDC8 as Red List (low evidence)","entity_name":"CCDC8","entity_type":"gene"},{"created":"2019-12-06T21:37:58.109681+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.762","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc8 has been classified as Red List (Low Evidence).","entity_name":"CCDC8","entity_type":"gene"},{"created":"2019-12-06T21:37:24.620479+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.761","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CCDC78 as ready","entity_name":"CCDC78","entity_type":"gene"},{"created":"2019-12-06T21:37:24.613282+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.761","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc78 has been classified as Amber List (Moderate Evidence).","entity_name":"CCDC78","entity_type":"gene"},{"created":"2019-12-06T21:37:19.850442+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.761","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CCDC78 were changed from  to Centronuclear myopathy 4, MIM#614807","entity_name":"CCDC78","entity_type":"gene"},{"created":"2019-12-06T21:37:07.334885+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.760","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CCDC78 were set to ","entity_name":"CCDC78","entity_type":"gene"},{"created":"2019-12-06T21:36:58.655452+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.759","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CCDC78 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CCDC78","entity_type":"gene"},{"created":"2019-12-06T21:36:47.892790+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.758","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CCDC78 as Amber List (moderate evidence)","entity_name":"CCDC78","entity_type":"gene"},{"created":"2019-12-06T21:36:47.877347+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.758","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc78 has been classified as Amber List (Moderate Evidence).","entity_name":"CCDC78","entity_type":"gene"},{"created":"2019-12-06T21:36:16.522975+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.757","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CACNA1G as ready","entity_name":"CACNA1G","entity_type":"gene"},{"created":"2019-12-06T21:36:16.515818+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.757","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cacna1g has been classified as Green List (High Evidence).","entity_name":"CACNA1G","entity_type":"gene"},{"created":"2019-12-06T21:36:11.891715+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.757","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CACNA1G were changed from  to Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits, MIM#618087","entity_name":"CACNA1G","entity_type":"gene"},{"created":"2019-12-06T21:35:59.471178+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.756","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CACNA1G were set to ","entity_name":"CACNA1G","entity_type":"gene"},{"created":"2019-12-06T21:35:50.327140+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.755","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CACNA1G was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CACNA1G","entity_type":"gene"},{"created":"2019-12-06T21:35:13.953930+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.754","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CA8 as ready","entity_name":"CA8","entity_type":"gene"},{"created":"2019-12-06T21:35:13.946744+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.754","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ca8 has been classified as Green List (High Evidence).","entity_name":"CA8","entity_type":"gene"},{"created":"2019-12-06T21:35:09.630566+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.754","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CA8 were changed from  to Cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3, MIM#613227","entity_name":"CA8","entity_type":"gene"},{"created":"2019-12-06T21:34:56.384274+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.753","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CA8 were set to ","entity_name":"CA8","entity_type":"gene"},{"created":"2019-12-06T21:34:43.004193+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.752","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CA8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CA8","entity_type":"gene"},{"created":"2019-12-06T21:34:13.959518+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.751","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CA2 as ready","entity_name":"CA2","entity_type":"gene"},{"created":"2019-12-06T21:34:13.951660+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.751","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ca2 has been classified as Green List (High Evidence).","entity_name":"CA2","entity_type":"gene"},{"created":"2019-12-06T21:34:09.198121+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.751","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CA2 were changed from  to Osteopetrosis, autosomal recessive 3, with renal tubular acidosis, MIM#259730","entity_name":"CA2","entity_type":"gene"},{"created":"2019-12-06T21:33:56.074207+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.750","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CA2","entity_type":"gene"},{"created":"2019-12-06T21:07:43.823741+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.749","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C3orf58 as ready","entity_name":"C3orf58","entity_type":"gene"},{"created":"2019-12-06T21:07:43.816517+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.749","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c3orf58 has been classified as Red List (Low Evidence).","entity_name":"C3orf58","entity_type":"gene"},{"created":"2019-12-06T21:07:38.791170+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.749","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: C3orf58 as Red List (low evidence)","entity_name":"C3orf58","entity_type":"gene"},{"created":"2019-12-06T21:07:38.782660+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.749","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c3orf58 has been classified as Red List (Low Evidence).","entity_name":"C3orf58","entity_type":"gene"},{"created":"2019-12-06T21:07:00.516212+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.748","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C19orf12 as ready","entity_name":"C19orf12","entity_type":"gene"},{"created":"2019-12-06T21:07:00.509028+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.748","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c19orf12 has been classified as Red List (Low Evidence).","entity_name":"C19orf12","entity_type":"gene"}]}