{"count":221415,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=361","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=359","results":[{"created":"2024-10-24T13:53:17.294213+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.384","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rtn4ip1 has been classified as Red List (Low Evidence).","entity_name":"RTN4IP1","entity_type":"gene"},{"created":"2024-10-24T13:52:20.027305+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.383","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNU7-1 as ready","entity_name":"RNU7-1","entity_type":"gene"},{"created":"2024-10-24T13:52:20.013418+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.383","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnu7-1 has been classified as Amber List (Moderate Evidence).","entity_name":"RNU7-1","entity_type":"gene"},{"created":"2024-10-24T13:52:14.465483+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.383","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RNU7-1 as Amber List (moderate evidence)","entity_name":"RNU7-1","entity_type":"gene"},{"created":"2024-10-24T13:52:14.451750+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.383","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnu7-1 has been classified as Amber List (Moderate Evidence).","entity_name":"RNU7-1","entity_type":"gene"},{"created":"2024-10-24T13:50:28.162879+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.382","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PUM1 as ready","entity_name":"PUM1","entity_type":"gene"},{"created":"2024-10-24T13:50:28.150779+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.382","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pum1 has been classified as Red List (Low Evidence).","entity_name":"PUM1","entity_type":"gene"},{"created":"2024-10-24T13:50:23.821947+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.382","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PUM1 as Red List (low evidence)","entity_name":"PUM1","entity_type":"gene"},{"created":"2024-10-24T13:50:23.797995+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.382","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pum1 has been classified as Red List (Low Evidence).","entity_name":"PUM1","entity_type":"gene"},{"created":"2024-10-24T13:49:36.393653+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.381","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PGAP2 as ready","entity_name":"PGAP2","entity_type":"gene"},{"created":"2024-10-24T13:49:36.377726+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.381","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pgap2 has been classified as Red List (Low Evidence).","entity_name":"PGAP2","entity_type":"gene"},{"created":"2024-10-24T13:45:40.811318+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.381","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PGAP2 as Red List (low evidence)","entity_name":"PGAP2","entity_type":"gene"},{"created":"2024-10-24T13:45:40.800651+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.381","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pgap2 has been classified as Red List (Low Evidence).","entity_name":"PGAP2","entity_type":"gene"},{"created":"2024-10-24T13:44:53.774961+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.380","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF5C as ready","entity_name":"KIF5C","entity_type":"gene"},{"created":"2024-10-24T13:44:53.762213+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.380","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif5c has been classified as Red List (Low Evidence).","entity_name":"KIF5C","entity_type":"gene"},{"created":"2024-10-24T13:44:46.960537+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.380","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIF5C as Red List (low evidence)","entity_name":"KIF5C","entity_type":"gene"},{"created":"2024-10-24T13:44:46.951214+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.380","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif5c has been classified as Red List (Low Evidence).","entity_name":"KIF5C","entity_type":"gene"},{"created":"2024-10-24T13:44:03.996076+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.379","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KCNK9 as ready","entity_name":"KCNK9","entity_type":"gene"},{"created":"2024-10-24T13:44:03.982426+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.379","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnk9 has been classified as Red List (Low Evidence).","entity_name":"KCNK9","entity_type":"gene"},{"created":"2024-10-24T13:43:51.078542+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.379","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KCNK9 as Red List (low evidence)","entity_name":"KCNK9","entity_type":"gene"},{"created":"2024-10-24T13:43:51.060802+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.379","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnk9 has been classified as Red List (Low Evidence).","entity_name":"KCNK9","entity_type":"gene"},{"created":"2024-10-24T13:43:07.852757+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.378","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IREB2 as ready","entity_name":"IREB2","entity_type":"gene"},{"created":"2024-10-24T13:43:07.838082+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.378","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ireb2 has been classified as Red List (Low Evidence).","entity_name":"IREB2","entity_type":"gene"},{"created":"2024-10-24T13:42:59.852081+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.378","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IREB2 as Red List (low evidence)","entity_name":"IREB2","entity_type":"gene"},{"created":"2024-10-24T13:42:59.813936+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.378","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ireb2 has been classified as Red List (Low Evidence).","entity_name":"IREB2","entity_type":"gene"},{"created":"2024-10-24T13:42:17.295983+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.377","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EBF3 as ready","entity_name":"EBF3","entity_type":"gene"},{"created":"2024-10-24T13:42:17.283377+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.377","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ebf3 has been classified as Red List (Low Evidence).","entity_name":"EBF3","entity_type":"gene"},{"created":"2024-10-24T13:42:08.901635+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.377","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EBF3 as Red List (low evidence)","entity_name":"EBF3","entity_type":"gene"},{"created":"2024-10-24T13:42:08.880935+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.377","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ebf3 has been classified as Red List (Low Evidence).","entity_name":"EBF3","entity_type":"gene"},{"created":"2024-10-24T13:41:22.809330+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.376","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COQ4 as ready","entity_name":"COQ4","entity_type":"gene"},{"created":"2024-10-24T13:41:22.798747+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.376","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq4 has been classified as Red List (Low Evidence).","entity_name":"COQ4","entity_type":"gene"},{"created":"2024-10-24T13:41:15.746868+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.376","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COQ4 as Red List (low evidence)","entity_name":"COQ4","entity_type":"gene"},{"created":"2024-10-24T13:41:15.730893+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.376","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: coq4 has been classified as Red List (Low Evidence).","entity_name":"COQ4","entity_type":"gene"},{"created":"2024-10-24T13:40:29.202419+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.375","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLN6 as ready","entity_name":"CLN6","entity_type":"gene"},{"created":"2024-10-24T13:40:29.175524+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.375","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cln6 has been classified as Red List (Low Evidence).","entity_name":"CLN6","entity_type":"gene"},{"created":"2024-10-24T13:40:18.494004+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.375","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CLN6 as Red List (low evidence)","entity_name":"CLN6","entity_type":"gene"},{"created":"2024-10-24T13:40:18.477176+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.375","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cln6 has been classified as Red List (Low Evidence).","entity_name":"CLN6","entity_type":"gene"},{"created":"2024-10-24T13:06:24.961418+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.374","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BRAF as Amber List (moderate evidence)","entity_name":"BRAF","entity_type":"gene"},{"created":"2024-10-24T13:06:24.943576+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.374","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: braf has been classified as Amber List (Moderate Evidence).","entity_name":"BRAF","entity_type":"gene"},{"created":"2024-10-24T13:06:16.148964+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.373","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRAF as ready","entity_name":"BRAF","entity_type":"gene"},{"created":"2024-10-24T13:06:16.114753+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.373","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: braf has been classified as Amber List (Moderate Evidence).","entity_name":"BRAF","entity_type":"gene"},{"created":"2024-10-24T13:04:26.376863+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.373","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BRAF as Amber List (moderate evidence)","entity_name":"BRAF","entity_type":"gene"},{"created":"2024-10-24T13:04:26.339816+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.373","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: braf has been classified as Amber List (Moderate Evidence).","entity_name":"BRAF","entity_type":"gene"},{"created":"2024-10-24T13:01:14.078119+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.372","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALDH7A1 as ready","entity_name":"ALDH7A1","entity_type":"gene"},{"created":"2024-10-24T13:01:14.049038+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.372","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aldh7a1 has been classified as Red List (Low Evidence).","entity_name":"ALDH7A1","entity_type":"gene"},{"created":"2024-10-24T13:01:08.911044+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.372","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ALDH7A1 as Red List (low evidence)","entity_name":"ALDH7A1","entity_type":"gene"},{"created":"2024-10-24T13:01:08.890140+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.372","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aldh7a1 has been classified as Red List (Low Evidence).","entity_name":"ALDH7A1","entity_type":"gene"},{"created":"2024-10-24T13:00:00.150994+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.371","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PIK3CA as Red List (low evidence)","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2024-10-24T13:00:00.134263+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.371","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pik3ca has been classified as Red List (Low Evidence).","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2024-10-24T12:59:36.349452+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.371","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIK3CA as ready","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2024-10-24T12:59:36.329402+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.371","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pik3ca has been classified as Red List (Low Evidence).","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2024-10-24T12:59:28.349058+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.371","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PIK3CA as Red List (low evidence)","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2024-10-24T12:59:28.323665+11:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.371","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pik3ca has been classified as Red List (Low Evidence).","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2024-10-24T10:37:58.531712+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.471","user_name":"Michelle Torres","item_type":"entity","text":"reviewed gene: ADAMTSL2: Rating: GREEN; Mode of pathogenicity: None; Publications: 20301776, 38300707; Phenotypes: Geleophysic dysplasia 1 MIM#231050; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ADAMTSL2","entity_type":"gene"},{"created":"2024-10-24T09:59:22.858774+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.471","user_name":"Michelle Torres","item_type":"entity","text":"reviewed gene: ADA: Rating: GREEN; Mode of pathogenicity: None; Publications: 20301656, 8673127; Phenotypes: Severe combined immunodeficiency due to ADA deficiency MIM#102700 AR, Smo, Adenosine deaminase deficiency, partial MIM#102700 AR,SMo.; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ADA","entity_type":"gene"},{"created":"2024-10-23T21:03:18.319463+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.471","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAT as ready","entity_name":"LAT","entity_type":"gene"},{"created":"2024-10-23T21:03:18.305594+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.471","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lat has been classified as Green List (High Evidence).","entity_name":"LAT","entity_type":"gene"},{"created":"2024-10-23T21:03:10.985153+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.471","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LAT were set to 27522155; 27242165","entity_name":"LAT","entity_type":"gene"},{"created":"2024-10-23T21:02:53.765699+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.470","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LAT: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Immunodeficiency 52, MIM# 617514, severe combined immunodeficiency due to LAT deficiency MONDO:0044721; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAT","entity_type":"gene"},{"created":"2024-10-23T21:00:59.313360+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6579","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF5A as ready","entity_name":"KIF5A","entity_type":"gene"},{"created":"2024-10-23T21:00:59.293526+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6579","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif5a has been classified as Amber List (Moderate Evidence).","entity_name":"KIF5A","entity_type":"gene"},{"created":"2024-10-23T21:00:55.729314+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6579","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF5A were changed from Spastic paraplegia 10, autosomal dominant, MIM# 604187; inherited neurodegenerative disorder MONDO:0024237 to Spastic paraplegia 10, autosomal dominant, MIM# 604187; inherited neurodegenerative disorder MONDO:0024237","entity_name":"KIF5A","entity_type":"gene"},{"created":"2024-10-23T21:00:33.762696+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2069","user_name":"Achchuthan Shanmugasundram","item_type":"entity","text":"gene: AJAP1 was added\ngene: AJAP1 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: AJAP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: AJAP1 were set to 38985877\nPhenotypes for gene: AJAP1 were set to neurodevelopmental disorder, MONDO:0700092\nReview for gene: AJAP1 was set to GREEN\nAdded comment: PMID:38985877 reported five unrelated individuals with monoallelic variants or a deletion in AJAP1 gene and they presented with epilepsy, neurodevelopmental problems, or intellectual disability. There is also supporting functional evidence available. \nSources: Literature","entity_name":"AJAP1","entity_type":"gene"},{"created":"2024-10-23T21:00:11.694863+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6578","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF5A were changed from  to Spastic paraplegia 10, autosomal dominant, MIM# 604187; inherited neurodegenerative disorder MONDO:0024237","entity_name":"KIF5A","entity_type":"gene"},{"created":"2024-10-23T20:59:26.231378+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6577","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF5A were set to 18853458","entity_name":"KIF5A","entity_type":"gene"},{"created":"2024-10-23T20:58:44.943026+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6576","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF5A were set to ","entity_name":"KIF5A","entity_type":"gene"},{"created":"2024-10-23T20:57:57.077017+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6575","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIF5A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF5A","entity_type":"gene"},{"created":"2024-10-23T20:57:25.197684+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6574","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIF5A as Amber List (moderate evidence)","entity_name":"KIF5A","entity_type":"gene"},{"created":"2024-10-23T20:57:25.188387+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6574","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif5a has been classified as Amber List (Moderate Evidence).","entity_name":"KIF5A","entity_type":"gene"},{"created":"2024-10-23T20:56:29.545199+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6573","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIF5A as Amber List (moderate evidence)","entity_name":"KIF5A","entity_type":"gene"},{"created":"2024-10-23T20:56:29.523179+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6573","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif5a has been classified as Amber List (Moderate Evidence).","entity_name":"KIF5A","entity_type":"gene"},{"created":"2024-10-23T20:54:42.346644+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6572","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF7 as ready","entity_name":"KIF7","entity_type":"gene"},{"created":"2024-10-23T20:54:42.336710+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6572","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif7 has been classified as Green List (High Evidence).","entity_name":"KIF7","entity_type":"gene"},{"created":"2024-10-23T20:54:32.838330+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6572","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF7 were changed from acrocallosal syndrome MONDO:0008708; KIF7-related ciliopathy MONDO:0800463; Joubert syndrome 12 MIM#200990 to acrocallosal syndrome MONDO:0008708; KIF7-related ciliopathy MONDO:0800463; Joubert syndrome 12 MIM#200990","entity_name":"KIF7","entity_type":"gene"},{"created":"2024-10-23T20:53:56.566535+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6571","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF7 were changed from  to acrocallosal syndrome MONDO:0008708; KIF7-related ciliopathy MONDO:0800463; Joubert syndrome 12 MIM#200990","entity_name":"KIF7","entity_type":"gene"},{"created":"2024-10-23T20:51:46.575759+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6570","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF7 were set to ","entity_name":"KIF7","entity_type":"gene"},{"created":"2024-10-23T20:51:09.461107+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6569","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIF7 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KIF7","entity_type":"gene"},{"created":"2024-10-23T20:50:26.160799+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6569","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIF7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KIF7","entity_type":"gene"},{"created":"2024-10-23T20:46:48.004492+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6568","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KLHL7 as ready","entity_name":"KLHL7","entity_type":"gene"},{"created":"2024-10-23T20:46:47.959067+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6568","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: klhl7 has been classified as Green List (High Evidence).","entity_name":"KLHL7","entity_type":"gene"},{"created":"2024-10-23T20:46:08.373352+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6568","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KLHL7 were changed from  to PERCHING syndrome MONDO:0014890; acrocallosal syndrome MONDO:0008708","entity_name":"KLHL7","entity_type":"gene"},{"created":"2024-10-23T20:45:18.785261+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6567","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KLHL7 were set to 27392078; 30142437; 29074562","entity_name":"KLHL7","entity_type":"gene"},{"created":"2024-10-23T20:44:35.434813+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6566","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KLHL7 were set to ","entity_name":"KLHL7","entity_type":"gene"},{"created":"2024-10-23T20:43:32.405972+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6565","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KLHL7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KLHL7","entity_type":"gene"},{"created":"2024-10-23T20:24:43.694323+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6564","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: L2HGDH as ready","entity_name":"L2HGDH","entity_type":"gene"},{"created":"2024-10-23T20:24:43.676111+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6564","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: l2hgdh has been classified as Green List (High Evidence).","entity_name":"L2HGDH","entity_type":"gene"},{"created":"2024-10-23T20:24:36.238349+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6564","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: L2HGDH were changed from  to L-2-hydroxyglutaric aciduria, MIM#236792","entity_name":"L2HGDH","entity_type":"gene"},{"created":"2024-10-23T20:23:38.215549+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6563","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: L2HGDH were set to ","entity_name":"L2HGDH","entity_type":"gene"},{"created":"2024-10-23T20:22:52.449569+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6562","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: L2HGDH was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"L2HGDH","entity_type":"gene"},{"created":"2024-10-23T20:22:17.593124+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6561","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: L2HGDH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"L2HGDH","entity_type":"gene"},{"created":"2024-10-23T20:21:09.446867+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6560","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMA1 as ready","entity_name":"LAMA1","entity_type":"gene"},{"created":"2024-10-23T20:21:09.434699+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6560","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lama1 has been classified as Green List (High Evidence).","entity_name":"LAMA1","entity_type":"gene"},{"created":"2024-10-23T20:20:35.538850+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6560","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LAMA1 were changed from  to ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome MONDO:0014419","entity_name":"LAMA1","entity_type":"gene"},{"created":"2024-10-23T20:19:54.906940+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6559","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LAMA1 were set to ","entity_name":"LAMA1","entity_type":"gene"},{"created":"2024-10-23T20:19:10.436809+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6558","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LAMA1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMA1","entity_type":"gene"},{"created":"2024-10-23T20:18:27.376699+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6557","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LAMA1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMA1","entity_type":"gene"},{"created":"2024-10-23T20:17:43.738830+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6556","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LAMA1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMA1","entity_type":"gene"},{"created":"2024-10-23T19:21:16.610215+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6555","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LAMA1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMA1","entity_type":"gene"},{"created":"2024-10-23T19:20:19.555771+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6554","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ISPD as ready","entity_name":"ISPD","entity_type":"gene"},{"created":"2024-10-23T19:20:19.541391+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6554","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ispd has been classified as Green List (High Evidence).","entity_name":"ISPD","entity_type":"gene"}]}