{"count":221415,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=547","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=545","results":[{"created":"2023-09-18T18:09:05.093029+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ABAT as Amber List (moderate evidence)","entity_name":"ABAT","entity_type":"gene"},{"created":"2023-09-18T18:09:05.079667+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: abat has been classified as Amber List (Moderate Evidence).","entity_name":"ABAT","entity_type":"gene"},{"created":"2023-09-18T18:08:21.597367+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDE2A were set to 32467598; 32196122; 29392776","entity_name":"PDE2A","entity_type":"gene"},{"created":"2023-09-18T18:07:28.784601+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: XPR1 as ready","entity_name":"XPR1","entity_type":"gene"},{"created":"2023-09-18T18:07:28.768277+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpr1 has been classified as Amber List (Moderate Evidence).","entity_name":"XPR1","entity_type":"gene"},{"created":"2023-09-18T18:07:26.042903+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: XPR1 were changed from brain calcification; basal ganglia calcification; paroxysmal dyskinesia; epilepsy; DEE to Basal ganglia calcification, idiopathic, 6, MIM# 616413; brain calcification; basal ganglia calcification; paroxysmal dyskinesia; epilepsy; DEE","entity_name":"XPR1","entity_type":"gene"},{"created":"2023-09-18T18:06:53.120427+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: XPR1 as Amber List (moderate evidence)","entity_name":"XPR1","entity_type":"gene"},{"created":"2023-09-18T18:06:53.109565+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpr1 has been classified as Amber List (Moderate Evidence).","entity_name":"XPR1","entity_type":"gene"},{"created":"2023-09-18T18:06:03.873197+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLDN5 as ready","entity_name":"CLDN5","entity_type":"gene"},{"created":"2023-09-18T18:06:03.857931+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cldn5 has been classified as Green List (High Evidence).","entity_name":"CLDN5","entity_type":"gene"},{"created":"2023-09-18T18:06:00.334083+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CLDN5 as Green List (high evidence)","entity_name":"CLDN5","entity_type":"gene"},{"created":"2023-09-18T18:06:00.323289+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cldn5 has been classified as Green List (High Evidence).","entity_name":"CLDN5","entity_type":"gene"},{"created":"2023-09-18T18:05:32.423647+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLDN5 were changed from familial migraine; alternating hemiplegia; hemiplegic migraine; brain calcification; acquired microcephaly; epilepsy to Syndromic disorder, MONDO:0002254, CLDN5-related; familial migraine; alternating hemiplegia; hemiplegic migraine; brain calcification; acquired microcephaly; epilepsy","entity_name":"CLDN5","entity_type":"gene"},{"created":"2023-09-18T18:05:08.406219+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CLDN5 as Green List (high evidence)","entity_name":"CLDN5","entity_type":"gene"},{"created":"2023-09-18T18:05:08.393112+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cldn5 has been classified as Green List (High Evidence).","entity_name":"CLDN5","entity_type":"gene"},{"created":"2023-09-18T18:04:08.445132+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIAA1161 as ready","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2023-09-18T18:04:08.434391+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiaa1161 has been classified as Green List (High Evidence).","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2023-09-18T18:04:05.447185+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIAA1161 were changed from paroxysmal dyskinesia; brain calcification; episodic hemiparesis to Basal ganglia calcification, idiopathic, 7, autosomal recessive, OMIM #618317; paroxysmal dyskinesia; brain calcification; episodic hemiparesis","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2023-09-18T18:03:21.800430+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIAA1161 as Green List (high evidence)","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2023-09-18T18:03:21.792123+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiaa1161 has been classified as Green List (High Evidence).","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2023-09-18T18:02:29.415296+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKN as ready","entity_name":"PRKN","entity_type":"gene"},{"created":"2023-09-18T18:02:29.406172+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkn has been classified as Amber List (Moderate Evidence).","entity_name":"PRKN","entity_type":"gene"},{"created":"2023-09-18T18:02:26.859109+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRKN were changed from paroxysmal exercise induced dyskinesia; fasting induced dyskinesia; early onset parkinsonism to Parkinson disease, juvenile, type 2 MIM#600116; paroxysmal exercise induced dyskinesia; fasting induced dyskinesia; early onset parkinsonism","entity_name":"PRKN","entity_type":"gene"},{"created":"2023-09-18T18:01:47.139346+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PRKN as Amber List (moderate evidence)","entity_name":"PRKN","entity_type":"gene"},{"created":"2023-09-18T18:01:47.124070+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkn has been classified as Amber List (Moderate Evidence).","entity_name":"PRKN","entity_type":"gene"},{"created":"2023-09-18T18:00:52.854028+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NBEA as ready","entity_name":"NBEA","entity_type":"gene"},{"created":"2023-09-18T18:00:52.842721+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nbea has been classified as Amber List (Moderate Evidence).","entity_name":"NBEA","entity_type":"gene"},{"created":"2023-09-18T18:00:37.867745+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NBEA were changed from Paroxysmal Kinesigenic Dyskinesia; DEE; autism; intellectual disability to Neurodevelopmental disorder with or without early-onset generalized epilepsy, MIM# 619157; Paroxysmal Kinesigenic Dyskinesia; DEE; autism; intellectual disability","entity_name":"NBEA","entity_type":"gene"},{"created":"2023-09-18T17:59:48.629762+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NBEA as Amber List (moderate evidence)","entity_name":"NBEA","entity_type":"gene"},{"created":"2023-09-18T17:59:48.621835+10:00","panel_name":"Paroxysmal Dyskinesia","panel_id":259,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nbea has been classified as Amber List (Moderate Evidence).","entity_name":"NBEA","entity_type":"gene"},{"created":"2023-09-18T17:58:51.592696+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5472","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB3 as ready","entity_name":"TUBB3","entity_type":"gene"},{"created":"2023-09-18T17:58:51.578693+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5472","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb3 has been classified as Green List (High Evidence).","entity_name":"TUBB3","entity_type":"gene"},{"created":"2023-09-18T17:57:55.508748+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5472","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBB3 were changed from  to complex cortical dysplasia with other brain malformations 1 MONDO:0013541","entity_name":"TUBB3","entity_type":"gene"},{"created":"2023-09-18T17:57:11.749323+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5471","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB3 were set to ","entity_name":"TUBB3","entity_type":"gene"},{"created":"2023-09-18T17:53:42.387442+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5470","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBB3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB3","entity_type":"gene"},{"created":"2023-09-18T17:48:10.272362+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5469","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB4A as ready","entity_name":"TUBB4A","entity_type":"gene"},{"created":"2023-09-18T17:48:10.260591+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5469","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb4a has been classified as Green List (High Evidence).","entity_name":"TUBB4A","entity_type":"gene"},{"created":"2023-09-18T17:47:11.372913+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5469","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBB4A were changed from  to hypomyelinating leukodystrophy 6 MONDO:0012905","entity_name":"TUBB4A","entity_type":"gene"},{"created":"2023-09-18T17:46:25.174142+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5468","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB4A were set to ","entity_name":"TUBB4A","entity_type":"gene"},{"created":"2023-09-18T16:36:30.795609+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5467","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBB4A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB4A","entity_type":"gene"},{"created":"2023-09-18T16:30:21.620656+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5466","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TH as ready","entity_name":"TH","entity_type":"gene"},{"created":"2023-09-18T16:30:21.610337+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5466","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: th has been classified as Green List (High Evidence).","entity_name":"TH","entity_type":"gene"},{"created":"2023-09-18T16:30:16.133811+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5466","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TH were changed from  to Segawa syndrome, recessive MIM#605407","entity_name":"TH","entity_type":"gene"},{"created":"2023-09-18T16:29:42.009204+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5465","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TH were set to ","entity_name":"TH","entity_type":"gene"},{"created":"2023-09-18T16:28:39.911482+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5464","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TH","entity_type":"gene"},{"created":"2023-09-18T16:28:05.589557+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5463","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: TH.","entity_name":"TH","entity_type":"gene"},{"created":"2023-09-18T16:27:34.854646+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5463","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PTEN as ready","entity_name":"PTEN","entity_type":"gene"},{"created":"2023-09-18T16:27:34.840411+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5463","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pten has been classified as Green List (High Evidence).","entity_name":"PTEN","entity_type":"gene"},{"created":"2023-09-18T16:26:59.403617+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5463","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PTEN were changed from  to Cowden syndrome 1 MIM#158350; Macrocephaly/autism syndrome MIM#605309","entity_name":"PTEN","entity_type":"gene"},{"created":"2023-09-18T16:24:50.671325+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5462","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PTEN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PTEN","entity_type":"gene"},{"created":"2023-09-18T16:23:58.798364+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5461","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBG1 as ready","entity_name":"TUBG1","entity_type":"gene"},{"created":"2023-09-18T16:23:58.788936+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5461","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubg1 has been classified as Green List (High Evidence).","entity_name":"TUBG1","entity_type":"gene"},{"created":"2023-09-18T16:23:54.241193+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5461","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBG1 were changed from  to complex cortical dysplasia with other brain malformations 4 MONDO:0014171","entity_name":"TUBG1","entity_type":"gene"},{"created":"2023-09-18T16:23:15.954523+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5460","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBG1 were set to ","entity_name":"TUBG1","entity_type":"gene"},{"created":"2023-09-18T16:22:41.566562+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5459","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBG1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBG1","entity_type":"gene"},{"created":"2023-09-18T16:21:56.244992+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5458","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TWIST1 as ready","entity_name":"TWIST1","entity_type":"gene"},{"created":"2023-09-18T16:21:56.225515+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5458","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: twist1 has been classified as Green List (High Evidence).","entity_name":"TWIST1","entity_type":"gene"},{"created":"2023-09-18T16:21:50.911265+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5458","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TWIST1 were changed from  to Saethre-Chotzen syndrome MONDO:0007042","entity_name":"TWIST1","entity_type":"gene"},{"created":"2023-09-18T16:21:16.759649+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5457","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TWIST1 were set to ","entity_name":"TWIST1","entity_type":"gene"},{"created":"2023-09-18T16:20:39.028471+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5456","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TWIST1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TWIST1","entity_type":"gene"},{"created":"2023-09-18T16:19:53.438988+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5455","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBA5 as ready","entity_name":"UBA5","entity_type":"gene"},{"created":"2023-09-18T16:19:53.427516+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5455","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uba5 has been classified as Green List (High Evidence).","entity_name":"UBA5","entity_type":"gene"},{"created":"2023-09-18T16:19:49.110400+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5455","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBA5 were changed from  to Epileptic encephalopathy, early infantile, 44 (MIM#617132)","entity_name":"UBA5","entity_type":"gene"},{"created":"2023-09-18T16:19:21.292681+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5454","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBA5 were set to 33811063","entity_name":"UBA5","entity_type":"gene"},{"created":"2023-09-18T16:18:48.313027+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5453","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBA5 were set to ","entity_name":"UBA5","entity_type":"gene"},{"created":"2023-09-18T16:18:15.356000+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5452","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UBA5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"UBA5","entity_type":"gene"},{"created":"2023-09-18T16:17:31.982718+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5451","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBE3A as ready","entity_name":"UBE3A","entity_type":"gene"},{"created":"2023-09-18T16:17:31.971451+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5451","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ube3a has been classified as Green List (High Evidence).","entity_name":"UBE3A","entity_type":"gene"},{"created":"2023-09-18T16:17:28.022375+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5451","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBE3A were changed from  to Angelman syndrome MONDO:0007113","entity_name":"UBE3A","entity_type":"gene"},{"created":"2023-09-18T16:16:55.235529+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5450","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBE3A were set to ","entity_name":"UBE3A","entity_type":"gene"},{"created":"2023-09-18T16:16:22.332807+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5449","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UBE3A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)","entity_name":"UBE3A","entity_type":"gene"},{"created":"2023-09-18T16:15:31.068544+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5448","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SDHA as ready","entity_name":"SDHA","entity_type":"gene"},{"created":"2023-09-18T16:15:31.056256+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5448","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sdha has been classified as Green List (High Evidence).","entity_name":"SDHA","entity_type":"gene"},{"created":"2023-09-18T15:57:08.763403+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5448","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SDHA were changed from  to Mitochondrial complex II deficiency, nuclear type 1 MIM#252011","entity_name":"SDHA","entity_type":"gene"},{"created":"2023-09-18T15:56:29.450361+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5447","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SDHA were set to ","entity_name":"SDHA","entity_type":"gene"},{"created":"2023-09-18T15:55:49.270433+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5446","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SDHA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SDHA","entity_type":"gene"},{"created":"2023-09-18T15:54:58.850934+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5445","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VLDLR as ready","entity_name":"VLDLR","entity_type":"gene"},{"created":"2023-09-18T15:54:58.840489+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5445","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vldlr has been classified as Green List (High Evidence).","entity_name":"VLDLR","entity_type":"gene"},{"created":"2023-09-18T15:54:46.786705+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5445","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VLDLR were changed from  to cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1 MONDO:0024542","entity_name":"VLDLR","entity_type":"gene"},{"created":"2023-09-18T15:52:01.209565+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5444","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VLDLR were set to ","entity_name":"VLDLR","entity_type":"gene"},{"created":"2023-09-18T15:51:28.075105+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5443","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VLDLR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VLDLR","entity_type":"gene"},{"created":"2023-09-18T15:50:39.588693+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5442","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VPS13B as ready","entity_name":"VPS13B","entity_type":"gene"},{"created":"2023-09-18T15:50:39.577860+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5442","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps13b has been classified as Green List (High Evidence).","entity_name":"VPS13B","entity_type":"gene"},{"created":"2023-09-18T15:50:31.656489+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5442","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VPS13B were changed from  to Cohen syndrome MONDO:0008999","entity_name":"VPS13B","entity_type":"gene"},{"created":"2023-09-18T15:49:58.298352+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5441","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VPS13B were set to ","entity_name":"VPS13B","entity_type":"gene"},{"created":"2023-09-18T15:49:25.698855+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5440","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VPS13B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VPS13B","entity_type":"gene"},{"created":"2023-09-18T14:52:45.529575+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1173","user_name":"Lucy Spencer","item_type":"entity","text":"reviewed gene: SEMA3E: Rating: AMBER; Mode of pathogenicity: None; Publications: 15235037, 31691538, 31464029, 35628442, 32441320; Phenotypes: CHARGE syndrome MONDO:0008965, SEMA3E-related; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SEMA3E","entity_type":"gene"},{"created":"2023-09-17T15:55:59.502447+10:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.144","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SCAF4 were changed from Neurodevelopmental disorder MONDO#0700092, SCAF4-related to Fliedner-Zweier syndrome, MIM#620511","entity_name":"SCAF4","entity_type":"gene"},{"created":"2023-09-17T15:55:44.874444+10:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.143","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SCAF4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fliedner-Zweier syndrome, MIM#620511; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SCAF4","entity_type":"gene"},{"created":"2023-09-17T15:55:25.898658+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5439","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SCAF4 were changed from Mild intellectual disability; seizures; behavioral abnormalities to Fliedner-Zweier syndrome, MIM#620511","entity_name":"SCAF4","entity_type":"gene"},{"created":"2023-09-17T15:54:51.863088+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5438","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SCAF4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fliedner-Zweier syndrome, MIM#620511; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SCAF4","entity_type":"gene"},{"created":"2023-09-17T15:54:32.995828+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1917","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SCAF4 were changed from Mild intellectual disability; seizures; behavioral abnormalities to Fliedner-Zweier syndrome, MIM#620511","entity_name":"SCAF4","entity_type":"gene"},{"created":"2023-09-17T15:53:54.150304+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1916","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SCAF4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fliedner-Zweier syndrome, MIM#620511; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SCAF4","entity_type":"gene"},{"created":"2023-09-17T15:53:32.038752+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1173","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SCAF4 were changed from Mild intellectual disability; seizures; behavioral abnormalities to Fliedner-Zweier syndrome, MIM#620511","entity_name":"SCAF4","entity_type":"gene"},{"created":"2023-09-17T15:53:06.569471+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.1172","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SCAF4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fliedner-Zweier syndrome, MIM#620511; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SCAF4","entity_type":"gene"},{"created":"2023-09-16T16:47:31.047674+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5438","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VRK1 as ready","entity_name":"VRK1","entity_type":"gene"},{"created":"2023-09-16T16:47:31.034798+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5438","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vrk1 has been classified as Green List (High Evidence).","entity_name":"VRK1","entity_type":"gene"},{"created":"2023-09-16T16:44:02.553914+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5438","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VRK1 were changed from  to pontocerebellar hypoplasia type 1A MONDO:0011866","entity_name":"VRK1","entity_type":"gene"},{"created":"2023-09-16T16:43:20.850117+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5437","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VRK1 were set to ","entity_name":"VRK1","entity_type":"gene"},{"created":"2023-09-16T16:42:53.568824+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.5436","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VRK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VRK1","entity_type":"gene"}]}