{"count":221284,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=232","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=230","results":[{"created":"2025-05-09T13:44:16.992068+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.614","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: manba has been classified as Green List (High Evidence).","entity_name":"MANBA","entity_type":"gene"},{"created":"2025-05-09T13:44:10.590263+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.614","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MANBA were changed from Mannosidosis, beta, 248510 (3) to Mannosidosis, beta, MIM#248510","entity_name":"MANBA","entity_type":"gene"},{"created":"2025-05-09T13:43:47.254495+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.613","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAN2B1 as ready","entity_name":"MAN2B1","entity_type":"gene"},{"created":"2025-05-09T13:43:47.243055+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.613","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: man2b1 has been classified as Green List (High Evidence).","entity_name":"MAN2B1","entity_type":"gene"},{"created":"2025-05-09T13:43:45.193054+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.613","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAN2B1 were changed from Mannosidosis, alpha-, types I and II, 248500 (3) to Mannosidosis, alpha-, types I and II, MIM# 248500; MONDO:0009561","entity_name":"MAN2B1","entity_type":"gene"},{"created":"2025-05-09T10:43:35.190839+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.141","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LSM1 were changed from Neurodevelopmental disorder, MONDO:0700092, LSM1-related to FICUS syndrome, MIM# 621193","entity_name":"LSM1","entity_type":"gene"},{"created":"2025-05-09T10:43:06.923991+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.140","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LSM1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: FICUS syndrome, MIM# 621193; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LSM1","entity_type":"gene"},{"created":"2025-05-09T10:42:46.148794+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2588","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LSM1 were changed from Neurodevelopmental disorder, MONDO:0700092, LSM1-related to FICUS syndrome, MIM# 621193","entity_name":"LSM1","entity_type":"gene"},{"created":"2025-05-09T10:42:26.016773+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2587","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: LSM1: Changed phenotypes: FICUS syndrome, MIM# 621193","entity_name":"LSM1","entity_type":"gene"},{"created":"2025-05-09T09:58:48.646240+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.612","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: ZDHHC9 as ready","entity_name":"ZDHHC9","entity_type":"gene"},{"created":"2025-05-09T09:58:48.639180+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.612","user_name":"Seb Lunke","item_type":"entity","text":"Gene: zdhhc9 has been classified as Green List (High Evidence).","entity_name":"ZDHHC9","entity_type":"gene"},{"created":"2025-05-09T09:58:27.263376+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.612","user_name":"Seb Lunke","item_type":"entity","text":"Tag SV/CNV tag was added to gene: ZDHHC9.","entity_name":"ZDHHC9","entity_type":"gene"},{"created":"2025-05-09T09:58:02.482765+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.612","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: ZDHHC9 were changed from Mental retardation, X-linked syndromic, Raymond type, 300799 (3) to Syndromic X-linked intellectual disability, Raymond type MIM#300799 MONDO:0010427","entity_name":"ZDHHC9","entity_type":"gene"},{"created":"2025-05-09T09:57:54.068456+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.611","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: ZDHHC9 were set to ","entity_name":"ZDHHC9","entity_type":"gene"},{"created":"2025-05-09T09:56:50.596532+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.610","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: ZFYVE26 as ready","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2025-05-09T09:56:50.586727+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.610","user_name":"Seb Lunke","item_type":"entity","text":"Gene: zfyve26 has been classified as Green List (High Evidence).","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2025-05-09T09:56:46.842025+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.610","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: ZFYVE26 were changed from Spastic paraplegia 15, autosomal recessive, 270700 (3) to Spastic paraplegia 15, autosomal recessive MIM#270700","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2025-05-09T09:56:37.291586+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.609","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: ZFYVE26 were set to ","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2025-05-09T09:56:10.529150+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.608","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: ZNF711 as ready","entity_name":"ZNF711","entity_type":"gene"},{"created":"2025-05-09T09:56:10.519680+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.608","user_name":"Seb Lunke","item_type":"entity","text":"Gene: znf711 has been classified as Green List (High Evidence).","entity_name":"ZNF711","entity_type":"gene"},{"created":"2025-05-09T09:56:07.208155+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.608","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: ZNF711 were changed from Mental retardation, X-linked 97, 300803 (3) to Intellectual developmental disorder, X-linked 97, MIM# 300803","entity_name":"ZNF711","entity_type":"gene"},{"created":"2025-05-08T17:32:25.477644+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.12","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review was removed from gene: PUS7.","entity_name":"PUS7","entity_type":"gene"},{"created":"2025-05-08T17:32:12.264569+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.12","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review was removed from gene: PEX19.","entity_name":"PEX19","entity_type":"gene"},{"created":"2025-05-08T17:22:48.662143+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.12","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF469 as Green List (high evidence)","entity_name":"ZNF469","entity_type":"gene"},{"created":"2025-05-08T17:22:48.655736+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf469 has been classified as Green List (High Evidence).","entity_name":"ZNF469","entity_type":"gene"},{"created":"2025-05-08T17:22:42.006828+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.11","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review was removed from gene: ZNF469.","entity_name":"ZNF469","entity_type":"gene"},{"created":"2025-05-08T17:22:27.354754+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.11","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRAPPC12 as Green List (high evidence)","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2025-05-08T17:22:27.345027+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.11","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trappc12 has been classified as Green List (High Evidence).","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2025-05-08T17:22:20.033063+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.10","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review was removed from gene: TRAPPC12.","entity_name":"TRAPPC12","entity_type":"gene"},{"created":"2025-05-08T17:22:03.033369+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.10","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PUS7 as Green List (high evidence)","entity_name":"PUS7","entity_type":"gene"},{"created":"2025-05-08T17:22:03.023502+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pus7 has been classified as Green List (High Evidence).","entity_name":"PUS7","entity_type":"gene"},{"created":"2025-05-08T17:21:37.096706+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.9","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review was removed from gene: PTPN23.","entity_name":"PTPN23","entity_type":"gene"},{"created":"2025-05-08T17:21:32.083306+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.9","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PTPN23 as Green List (high evidence)","entity_name":"PTPN23","entity_type":"gene"},{"created":"2025-05-08T17:21:32.075205+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ptpn23 has been classified as Green List (High Evidence).","entity_name":"PTPN23","entity_type":"gene"},{"created":"2025-05-08T17:21:13.104910+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"2.8","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review was removed from gene: GPR143.","entity_name":"GPR143","entity_type":"gene"},{"created":"2025-05-08T17:20:09.575758+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.607","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LZTFL1 as ready","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2025-05-08T17:20:09.569421+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.607","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lztfl1 has been classified as Green List (High Evidence).","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2025-05-08T17:20:07.161401+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.607","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LZTFL1 were changed from Bardet-Biedl syndrome 17, 615994 (3) to Bardet-Biedl syndrome 17 MIM#615994; MONDO:0014445","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2025-05-08T17:19:56.245080+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.606","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LZTFL1 were set to ","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2025-05-08T17:19:36.598802+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.605","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LYST as ready","entity_name":"LYST","entity_type":"gene"},{"created":"2025-05-08T17:19:36.588274+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.605","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lyst has been classified as Green List (High Evidence).","entity_name":"LYST","entity_type":"gene"},{"created":"2025-05-08T17:19:34.124757+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.605","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LYST were changed from Chediak-Higashi syndrome, 214500 (3) to Chediak-Higashi syndrome MIM#214500","entity_name":"LYST","entity_type":"gene"},{"created":"2025-05-08T17:19:24.342169+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.604","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LYST were set to ","entity_name":"LYST","entity_type":"gene"},{"created":"2025-05-08T17:19:05.489692+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.603","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRPPRC as ready","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2025-05-08T17:19:05.480274+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.603","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrpprc has been classified as Green List (High Evidence).","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2025-05-08T17:19:02.736784+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.603","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRPPRC were changed from Leigh syndrome, French-Canadian type, 220111 (3) to Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian) 220111 (3)","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2025-05-08T17:18:51.408954+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.602","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LRPPRC were set to ","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2025-05-08T17:18:32.618117+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.601","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRP2 as ready","entity_name":"LRP2","entity_type":"gene"},{"created":"2025-05-08T17:18:32.611658+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.601","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrp2 has been classified as Green List (High Evidence).","entity_name":"LRP2","entity_type":"gene"},{"created":"2025-05-08T17:18:30.033350+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.601","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRP2 were changed from Donnai-Barrow syndrome, 222448 (3) to Donnai-Barrow syndrome, MIM #222448","entity_name":"LRP2","entity_type":"gene"},{"created":"2025-05-08T17:18:20.957008+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.600","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LRP2 were set to ","entity_name":"LRP2","entity_type":"gene"},{"created":"2025-05-08T17:18:00.828526+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.599","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRAT as ready","entity_name":"LRAT","entity_type":"gene"},{"created":"2025-05-08T17:18:00.818923+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.599","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrat has been classified as Green List (High Evidence).","entity_name":"LRAT","entity_type":"gene"},{"created":"2025-05-08T17:17:58.216075+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.599","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRAT were changed from Leber congenital amaurosis 14, 613341 (3) to Retinal dystrophy, early-onset severe; Leber congenital amaurosis 14; Retinitis pigmentosa, juvenile, all under MIM #613341","entity_name":"LRAT","entity_type":"gene"},{"created":"2025-05-08T17:17:46.095598+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.598","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LRAT were set to ","entity_name":"LRAT","entity_type":"gene"},{"created":"2025-05-08T17:12:14.639643+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.597","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LPL as ready","entity_name":"LPL","entity_type":"gene"},{"created":"2025-05-08T17:12:14.630624+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.597","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lpl has been classified as Green List (High Evidence).","entity_name":"LPL","entity_type":"gene"},{"created":"2025-05-08T17:12:12.174697+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.597","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LPL were changed from Lipoprotein lipase deficiency, 238600 (3) to Lipoprotein lipase deficiency MIM#238600","entity_name":"LPL","entity_type":"gene"},{"created":"2025-05-08T17:11:50.786092+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.596","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LMNA as ready","entity_name":"LMNA","entity_type":"gene"},{"created":"2025-05-08T17:11:50.779687+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.596","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lmna has been classified as Green List (High Evidence).","entity_name":"LMNA","entity_type":"gene"},{"created":"2025-05-08T17:11:46.857038+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.596","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LMNA were changed from Restrictive dermopathy, lethal, 275210 (3) to Restrictive dermopathy, lethal, MIM#275210; Mandibuloacral dysplasia, MIM# 248370","entity_name":"LMNA","entity_type":"gene"},{"created":"2025-05-08T17:11:07.431640+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.595","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LMBRD1 as ready","entity_name":"LMBRD1","entity_type":"gene"},{"created":"2025-05-08T17:11:07.421667+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.595","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lmbrd1 has been classified as Green List (High Evidence).","entity_name":"LMBRD1","entity_type":"gene"},{"created":"2025-05-08T17:11:05.037062+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.595","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LMBRD1 were changed from Methylmalonic aciduria and homocystinuria, cblF type, 277380 (3) to Methylmalonic aciduria and homocystinuria, cblF type, MIM#277380","entity_name":"LMBRD1","entity_type":"gene"},{"created":"2025-05-08T17:10:55.138238+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.594","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LMBRD1 were set to ","entity_name":"LMBRD1","entity_type":"gene"},{"created":"2025-05-08T17:10:35.869470+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.593","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LIPA as ready","entity_name":"LIPA","entity_type":"gene"},{"created":"2025-05-08T17:10:35.862925+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.593","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lipa has been classified as Green List (High Evidence).","entity_name":"LIPA","entity_type":"gene"},{"created":"2025-05-08T17:10:33.547760+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.593","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LIPA were changed from Cholesteryl ester storage disease, 278000 (3) to Wolman disease, MIM#620151; Cholesteryl ester storage disease, MIM#278000","entity_name":"LIPA","entity_type":"gene"},{"created":"2025-05-08T17:10:24.413134+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.592","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LIPA were set to ","entity_name":"LIPA","entity_type":"gene"},{"created":"2025-05-08T17:10:04.102857+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.591","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LIG4 as ready","entity_name":"LIG4","entity_type":"gene"},{"created":"2025-05-08T17:10:04.090570+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.591","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lig4 has been classified as Green List (High Evidence).","entity_name":"LIG4","entity_type":"gene"},{"created":"2025-05-08T17:10:01.942438+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.591","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LIG4 were changed from LIG4 syndrome, 606593 (3) to LIG4 syndrome, MIM# 606593 DNA ligase IV deficiency, MONDO:0011686","entity_name":"LIG4","entity_type":"gene"},{"created":"2025-05-08T17:09:47.798148+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.590","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LIG4 were set to ","entity_name":"LIG4","entity_type":"gene"},{"created":"2025-05-08T17:09:26.649924+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.589","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LIFR as ready","entity_name":"LIFR","entity_type":"gene"},{"created":"2025-05-08T17:09:26.640613+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.589","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lifr has been classified as Green List (High Evidence).","entity_name":"LIFR","entity_type":"gene"},{"created":"2025-05-08T17:09:24.251351+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.589","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LIFR were changed from Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome, 601559 (3) to Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome, MIM#601559","entity_name":"LIFR","entity_type":"gene"},{"created":"2025-05-08T17:09:13.018837+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.588","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LIFR were set to ","entity_name":"LIFR","entity_type":"gene"},{"created":"2025-05-08T17:08:52.571190+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.587","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LHX3 as ready","entity_name":"LHX3","entity_type":"gene"},{"created":"2025-05-08T17:08:52.565070+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.587","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lhx3 has been classified as Green List (High Evidence).","entity_name":"LHX3","entity_type":"gene"},{"created":"2025-05-08T17:08:50.241880+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.587","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LHX3 were changed from Pituitary hormone deficiency, combined, 3, 221750 (3) to Pituitary hormone deficiency, combined, 3 (MIM# 221750)","entity_name":"LHX3","entity_type":"gene"},{"created":"2025-05-08T17:08:39.844598+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.586","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LHX3 were set to ","entity_name":"LHX3","entity_type":"gene"},{"created":"2025-05-08T17:08:20.505006+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.585","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LDLRAP1 as ready","entity_name":"LDLRAP1","entity_type":"gene"},{"created":"2025-05-08T17:08:20.497369+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.585","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ldlrap1 has been classified as Green List (High Evidence).","entity_name":"LDLRAP1","entity_type":"gene"},{"created":"2025-05-08T17:08:18.536999+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.585","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LDLRAP1 were changed from Hypercholesterolemia, familial, autosomal recessive, 603813 (3) to Familial hypercholesterolemia 4, MIM#603813","entity_name":"LDLRAP1","entity_type":"gene"},{"created":"2025-05-08T17:08:08.283841+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.584","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LDLRAP1 were set to ","entity_name":"LDLRAP1","entity_type":"gene"},{"created":"2025-05-08T17:07:49.118033+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.583","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LDLR as ready","entity_name":"LDLR","entity_type":"gene"},{"created":"2025-05-08T17:07:49.111104+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.583","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ldlr has been classified as Green List (High Evidence).","entity_name":"LDLR","entity_type":"gene"},{"created":"2025-05-08T17:07:46.427679+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.583","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LDLR were changed from LDL cholesterol level QTL2/Hypercholesterolemia, familial to Hypercholesterolaemia, familial, 1, MIM# 143890","entity_name":"LDLR","entity_type":"gene"},{"created":"2025-05-08T17:07:17.917418+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.582","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LCA5 as ready","entity_name":"LCA5","entity_type":"gene"},{"created":"2025-05-08T17:07:17.910384+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.582","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lca5 has been classified as Green List (High Evidence).","entity_name":"LCA5","entity_type":"gene"},{"created":"2025-05-08T17:07:15.581768+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.582","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LCA5 were changed from Leber congenital amaurosis 5, 604537 (3) to Leber congenital amaurosis 5, MIM# 604537","entity_name":"LCA5","entity_type":"gene"},{"created":"2025-05-08T17:07:06.034512+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.581","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LCA5 were set to ","entity_name":"LCA5","entity_type":"gene"},{"created":"2025-05-08T17:06:44.765369+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.580","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: LARS.","entity_name":"LARS","entity_type":"gene"},{"created":"2025-05-08T17:06:36.116617+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.580","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LARS as ready","entity_name":"LARS","entity_type":"gene"},{"created":"2025-05-08T17:06:36.109855+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.580","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lars has been classified as Green List (High Evidence).","entity_name":"LARS","entity_type":"gene"},{"created":"2025-05-08T17:06:19.143596+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.580","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LARGE1 as ready","entity_name":"LARGE1","entity_type":"gene"},{"created":"2025-05-08T17:06:19.134485+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.580","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: large1 has been classified as Green List (High Evidence).","entity_name":"LARGE1","entity_type":"gene"},{"created":"2025-05-08T17:06:16.353372+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.580","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LARGE1 were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6, 613154 (3) to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, MIM #613154; Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6, MIM #608840","entity_name":"LARGE1","entity_type":"gene"},{"created":"2025-05-08T17:06:02.963710+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.579","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LARGE1 were set to ","entity_name":"LARGE1","entity_type":"gene"},{"created":"2025-05-08T17:05:42.254575+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.578","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMC2 as ready","entity_name":"LAMC2","entity_type":"gene"}]}