{"count":220751,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2003","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2001","results":[{"created":"2020-01-05T14:49:34.743075+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.652","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: h3f3a has been classified as Amber List (Moderate Evidence).","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:49:16.810370+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.651","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: H3F3A","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:49:03.106416+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: H3F3A as ready","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:49:03.098631+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: h3f3a has been classified as Amber List (Moderate Evidence).","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:48:58.627723+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: H3F3A as Amber List (moderate evidence)","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:48:58.621316+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: h3f3a has been classified as Amber List (Moderate Evidence).","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:48:23.509246+11:00","panel_name":"Regression_VCGS","panel_id":206,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: H3F3A","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:48:04.723382+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1506","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: H3F3A as ready","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:48:04.717364+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1506","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: h3f3a has been classified as Amber List (Moderate Evidence).","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:47:57.805710+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1506","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: H3F3A as Amber List (moderate evidence)","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:47:57.799697+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1506","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: h3f3a has been classified as Amber List (Moderate Evidence).","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:47:05.098811+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1505","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: H3F3B as Amber List (moderate evidence)","entity_name":"H3F3B","entity_type":"gene"},{"created":"2020-01-05T14:47:05.090786+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1505","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: h3f3b has been classified as Amber List (Moderate Evidence).","entity_name":"H3F3B","entity_type":"gene"},{"created":"2020-01-05T14:46:50.766997+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1504","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: H3F3B: Elizabeth J Bhoj, H3F3A/B Consortium, Hakon H. Hakonarson.: Mutations In H3f3a And H3f3b Encoding Histone 3.3: Report Of 26 Patients With Neurodevelopmental And Congenital Manifestations. American Society of Human Genetics, Orlando, FL October 2017 Notes: Platform Presentation.","entity_name":"H3F3B","entity_type":"gene"},{"created":"2020-01-05T14:46:16.415177+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1504","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: H3F3A","entity_name":"H3F3A","entity_type":"gene"},{"created":"2020-01-05T14:36:39.418533+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.651","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KAT5 as ready","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:36:39.415864+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.651","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Cannot find evidence for Mendelian gene-disease association.","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:36:39.391677+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.651","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kat5 has been classified as Red List (Low Evidence).","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:36:29.814142+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.651","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KAT5 as Red List (low evidence)","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:36:29.807918+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.651","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kat5 has been classified as Red List (Low Evidence).","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:36:01.243431+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KAT5 as ready","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:36:01.240498+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Cannot find evidence for Mendelian gene-disease association.","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:36:01.215115+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kat5 has been classified as Red List (Low Evidence).","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:35:56.661455+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KAT5 as Red List (low evidence)","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:35:56.655139+11:00","panel_name":"Cerebellar and Pontocerebellar hypoplasia_VCGS","panel_id":72,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kat5 has been classified as Red List (Low Evidence).","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:35:16.155515+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1504","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KAT5 as ready","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:35:16.152960+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1504","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Cannot find evidence for Mendelian gene-disease association.","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:35:16.126401+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1504","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kat5 has been classified as Red List (Low Evidence).","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:34:59.872509+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1504","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KAT5 as Red List (low evidence)","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T14:34:59.863973+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1504","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kat5 has been classified as Red List (Low Evidence).","entity_name":"KAT5","entity_type":"gene"},{"created":"2020-01-05T13:59:10.659176+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.650","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ROBO4 as ready","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:59:10.652280+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.650","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: robo4 has been classified as Green List (High Evidence).","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:59:01.292503+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.650","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ROBO4 as Green List (high evidence)","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:59:01.285420+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.650","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: robo4 has been classified as Green List (High Evidence).","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:58:41.642686+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.649","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ROBO4 was added\ngene: ROBO4 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: ROBO4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: ROBO4 were set to 30455415\nPhenotypes for gene: ROBO4 were set to bicuspid aortic valve; ascending aortic aneurysm; ascending aorta dilatation\nReview for gene: ROBO4 was set to GREEN\nAdded comment: Two families, functional data, incomplete penetrance. \nSources: Literature","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:56:18.503276+11:00","panel_name":"Congenital Heart Defect_VCGS","panel_id":76,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ROBO4 as ready","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:56:18.500512+11:00","panel_name":"Congenital Heart Defect_VCGS","panel_id":76,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Two families, functional data.","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:56:18.476727+11:00","panel_name":"Congenital Heart Defect_VCGS","panel_id":76,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: robo4 has been classified as Green List (High Evidence).","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:56:14.534095+11:00","panel_name":"Congenital Heart Defect_VCGS","panel_id":76,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ROBO4 as Green List (high evidence)","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:56:14.524614+11:00","panel_name":"Congenital Heart Defect_VCGS","panel_id":76,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: robo4 has been classified as Green List (High Evidence).","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:53:19.770755+11:00","panel_name":"Aortopathy, Connective tissue disorder_VCGS","panel_id":44,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ROBO4 as ready","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:53:19.764590+11:00","panel_name":"Aortopathy, Connective tissue disorder_VCGS","panel_id":44,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: robo4 has been classified as Green List (High Evidence).","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:53:07.304571+11:00","panel_name":"Aortopathy, Connective tissue disorder_VCGS","panel_id":44,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ROBO4 as Green List (high evidence)","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:53:07.294793+11:00","panel_name":"Aortopathy, Connective tissue disorder_VCGS","panel_id":44,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: robo4 has been classified as Green List (High Evidence).","entity_name":"ROBO4","entity_type":"gene"},{"created":"2020-01-05T13:39:13.472120+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MRPS16 as ready","entity_name":"MRPS16","entity_type":"gene"},{"created":"2020-01-05T13:39:13.458187+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mrps16 has been classified as Red List (Low Evidence).","entity_name":"MRPS16","entity_type":"gene"},{"created":"2020-01-05T13:38:39.272164+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MSH6 as ready","entity_name":"MSH6","entity_type":"gene"},{"created":"2020-01-05T13:38:39.265647+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: msh6 has been classified as Red List (Low Evidence).","entity_name":"MSH6","entity_type":"gene"},{"created":"2020-01-05T13:38:14.229247+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTM1 as ready","entity_name":"MTM1","entity_type":"gene"},{"created":"2020-01-05T13:38:14.221985+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mtm1 has been classified as Red List (Low Evidence).","entity_name":"MTM1","entity_type":"gene"},{"created":"2020-01-05T13:37:41.276652+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTMR2 as ready","entity_name":"MTMR2","entity_type":"gene"},{"created":"2020-01-05T13:37:41.267355+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mtmr2 has been classified as Red List (Low Evidence).","entity_name":"MTMR2","entity_type":"gene"},{"created":"2020-01-05T13:37:15.710181+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTPAP as ready","entity_name":"MTPAP","entity_type":"gene"},{"created":"2020-01-05T13:37:15.703672+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mtpap has been classified as Red List (Low Evidence).","entity_name":"MTPAP","entity_type":"gene"},{"created":"2020-01-05T13:36:39.152719+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYH3 as ready","entity_name":"MYH3","entity_type":"gene"},{"created":"2020-01-05T13:36:39.144062+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myh3 has been classified as Red List (Low Evidence).","entity_name":"MYH3","entity_type":"gene"},{"created":"2020-01-05T13:35:53.628172+11:00","panel_name":"Hydrocephalus/Ventriculomegaly_VCGS","panel_id":115,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYMK as ready","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:35:53.621590+11:00","panel_name":"Hydrocephalus/Ventriculomegaly_VCGS","panel_id":115,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mymk has been classified as Red List (Low Evidence).","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:35:46.280152+11:00","panel_name":"Hydrocephalus/Ventriculomegaly_VCGS","panel_id":115,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYMK were changed from  to Carey-Fineman-Ziter syndrome; OMIM #254940","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:35:19.223206+11:00","panel_name":"Hydrocephalus/Ventriculomegaly_VCGS","panel_id":115,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYMK were set to 28681861","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:34:51.984565+11:00","panel_name":"Hydrocephalus/Ventriculomegaly_VCGS","panel_id":115,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYMK were set to ","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:34:25.591107+11:00","panel_name":"Hydrocephalus/Ventriculomegaly_VCGS","panel_id":115,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYMK was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:33:58.441837+11:00","panel_name":"Hydrocephalus/Ventriculomegaly_VCGS","panel_id":115,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYMK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:33:23.582697+11:00","panel_name":"Hydrocephalus/Ventriculomegaly_VCGS","panel_id":115,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYMK as Red List (low evidence)","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:33:23.575925+11:00","panel_name":"Hydrocephalus/Ventriculomegaly_VCGS","panel_id":115,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mymk has been classified as Red List (Low Evidence).","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:32:48.333775+11:00","panel_name":"Hydrocephalus/Ventriculomegaly_VCGS","panel_id":115,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYMK: Rating: RED; Mode of pathogenicity: None; Publications: 28681861; Phenotypes: Carey-Fineman-Ziter syndrome, OMIM #254940; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:27:09.689888+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.648","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYMK as ready","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:27:09.683944+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.648","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mymk has been classified as Green List (High Evidence).","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:27:00.332922+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.648","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MYMK as Green List (high evidence)","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:27:00.326641+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.648","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mymk has been classified as Green List (High Evidence).","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:26:40.447926+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.647","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MYMK was added\ngene: MYMK was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: MYMK was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MYMK were set to 28681861\nPhenotypes for gene: MYMK were set to Carey-Fineman-Ziter syndrome; OMIM #254940\nReview for gene: MYMK was set to GREEN\nAdded comment: Sources: Expert list","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:23:46.171431+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYMK as ready","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:23:46.165669+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mymk has been classified as Red List (Low Evidence).","entity_name":"MYMK","entity_type":"gene"},{"created":"2020-01-05T13:23:04.910122+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO7A as ready","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-01-05T13:23:04.902946+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo7a has been classified as Red List (Low Evidence).","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-01-05T13:22:27.143060+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ORC4 as ready","entity_name":"ORC4","entity_type":"gene"},{"created":"2020-01-05T13:22:27.137141+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: orc4 has been classified as Red List (Low Evidence).","entity_name":"ORC4","entity_type":"gene"},{"created":"2020-01-05T13:21:52.612424+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ORC6 as ready","entity_name":"ORC6","entity_type":"gene"},{"created":"2020-01-05T13:21:52.606376+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: orc6 has been classified as Red List (Low Evidence).","entity_name":"ORC6","entity_type":"gene"},{"created":"2020-01-05T13:21:18.466192+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCBD1 as ready","entity_name":"PCBD1","entity_type":"gene"},{"created":"2020-01-05T13:21:18.460065+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcbd1 has been classified as Red List (Low Evidence).","entity_name":"PCBD1","entity_type":"gene"},{"created":"2020-01-05T13:19:39.151432+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC29A3 as ready","entity_name":"SLC29A3","entity_type":"gene"},{"created":"2020-01-05T13:19:39.145139+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc29a3 has been classified as Red List (Low Evidence).","entity_name":"SLC29A3","entity_type":"gene"},{"created":"2020-01-05T13:19:05.507301+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC2A10 as ready","entity_name":"SLC2A10","entity_type":"gene"},{"created":"2020-01-05T13:19:05.501248+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc2a10 has been classified as Red List (Low Evidence).","entity_name":"SLC2A10","entity_type":"gene"},{"created":"2020-01-05T13:18:28.840178+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC39A4 as ready","entity_name":"SLC39A4","entity_type":"gene"},{"created":"2020-01-05T13:18:28.834217+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc39a4 has been classified as Red List (Low Evidence).","entity_name":"SLC39A4","entity_type":"gene"},{"created":"2020-01-05T13:17:59.325135+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC5A2 as ready","entity_name":"SLC5A2","entity_type":"gene"},{"created":"2020-01-05T13:17:59.317141+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc5a2 has been classified as Red List (Low Evidence).","entity_name":"SLC5A2","entity_type":"gene"},{"created":"2020-01-05T13:16:14.712250+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMCHD1 as ready","entity_name":"SMCHD1","entity_type":"gene"},{"created":"2020-01-05T13:16:14.706703+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smchd1 has been classified as Red List (Low Evidence).","entity_name":"SMCHD1","entity_type":"gene"},{"created":"2020-01-05T13:15:07.549682+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMG6 as ready","entity_name":"SMG6","entity_type":"gene"},{"created":"2020-01-05T13:15:07.540202+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smg6 has been classified as Red List (Low Evidence).","entity_name":"SMG6","entity_type":"gene"},{"created":"2020-01-05T13:13:55.246503+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SNRPA as ready","entity_name":"SNRPA","entity_type":"gene"},{"created":"2020-01-05T13:13:55.234294+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snrpa has been classified as Red List (Low Evidence).","entity_name":"SNRPA","entity_type":"gene"},{"created":"2020-01-05T13:10:27.139333+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.646","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EDC3 as ready","entity_name":"EDC3","entity_type":"gene"},{"created":"2020-01-05T13:10:27.133102+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.646","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: edc3 has been classified as Red List (Low Evidence).","entity_name":"EDC3","entity_type":"gene"},{"created":"2020-01-05T13:10:15.373328+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.646","user_name":"Zornitza Stark","item_type":"entity","text":"gene: EDC3 was added\ngene: EDC3 was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: EDC3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: EDC3 were set to 29685133; 25701870\nPhenotypes for gene: EDC3 were set to Mental retardation, autosomal recessive 50, MIM#\t616460\nReview for gene: EDC3 was set to RED\nAdded comment: Single family reported; some functional data. \nSources: Expert list","entity_name":"EDC3","entity_type":"gene"},{"created":"2020-01-05T13:09:42.223504+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EDC3 as ready","entity_name":"EDC3","entity_type":"gene"},{"created":"2020-01-05T13:09:42.217146+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: edc3 has been classified as Red List (Low Evidence).","entity_name":"EDC3","entity_type":"gene"}]}