{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=920","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=918","results":[{"created":"2022-03-23T16:56:56.803459+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11819","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NEXN were changed from  to Lethal fetal cardiomyopathy; Hydrops fetalis; Cardiomyopathy, dilated 1CC - MIM#613122","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:54:06.600691+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11818","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NEXN were set to ","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:53:27.597426+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11817","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NEXN was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:52:53.414002+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEXN as ready","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:52:53.402448+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Red List (Low Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:52:50.478389+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.421","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NEXN were changed from  to Lethal fetal cardiomyopathy; Hydrops fetalis; Cardiomyopathy, dilated 1CC - MIM#613122","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:52:21.435638+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.420","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NEXN were set to ","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:51:45.469792+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.419","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NEXN was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:51:16.994774+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.418","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NEXN as Red List (low evidence)","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:51:16.983706+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.418","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Red List (Low Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:50:36.713164+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEXN as ready","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:50:36.704067+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Green List (High Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:50:00.886021+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NEXN as Green List (high evidence)","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:50:00.874130+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Green List (High Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:49:29.448770+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEXN as ready","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:49:29.430173+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Green List (High Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:48:28.217587+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NEXN as Green List (high evidence)","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:48:28.207055+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nexn has been classified as Green List (High Evidence).","entity_name":"NEXN","entity_type":"gene"},{"created":"2022-03-23T16:42:03.273703+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4583","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STX1B as ready","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:42:03.260274+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4583","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx1b has been classified as Green List (High Evidence).","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:41:56.457137+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4583","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STX1B were changed from  to Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:41:24.062098+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4582","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STX1B were set to ","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:40:49.147959+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4581","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: STX1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:40:12.963676+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4580","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STX1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 25362483, 33677401; Phenotypes: Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:38:54.186283+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STX1B as ready","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:38:54.172574+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx1b has been classified as Green List (High Evidence).","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:38:50.550648+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1503","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STX1B were changed from  to Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:38:05.805595+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1502","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STX1B were set to ","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:37:14.340271+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1501","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: STX1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:36:21.043760+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1500","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STX1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 25362483, 33677401; Phenotypes: Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:35:58.914387+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11816","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: STX1B: Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:35:26.595099+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11816","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STX1B as ready","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:35:26.583406+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11816","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx1b has been classified as Green List (High Evidence).","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:35:17.344578+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11816","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STX1B were changed from  to Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:34:55.740042+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11815","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STX1B were set to ","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:32:28.567712+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11814","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: STX1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:32:09.403488+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11813","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STX1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 25362483, 33677401; Phenotypes: Generalized epilepsy with febrile seizures plus, type 9, MIM# 616172; Mode of inheritance: None","entity_name":"STX1B","entity_type":"gene"},{"created":"2022-03-23T16:28:50.949819+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11813","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STX2 as ready","entity_name":"STX2","entity_type":"gene"},{"created":"2022-03-23T16:28:50.938421+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11813","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx2 has been classified as Red List (Low Evidence).","entity_name":"STX2","entity_type":"gene"},{"created":"2022-03-23T16:28:00.169782+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11813","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: STX2 as Red List (low evidence)","entity_name":"STX2","entity_type":"gene"},{"created":"2022-03-23T16:28:00.160462+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11813","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx2 has been classified as Red List (Low Evidence).","entity_name":"STX2","entity_type":"gene"},{"created":"2022-03-23T16:27:38.001358+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11812","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STX2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"STX2","entity_type":"gene"},{"created":"2022-03-23T16:26:19.743899+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11812","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STX4 as ready","entity_name":"STX4","entity_type":"gene"},{"created":"2022-03-23T16:26:19.734429+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11812","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx4 has been classified as Red List (Low Evidence).","entity_name":"STX4","entity_type":"gene"},{"created":"2022-03-23T16:26:08.605869+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11812","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: STX4 as Red List (low evidence)","entity_name":"STX4","entity_type":"gene"},{"created":"2022-03-23T16:26:08.593471+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11812","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx4 has been classified as Red List (Low Evidence).","entity_name":"STX4","entity_type":"gene"},{"created":"2022-03-23T16:25:49.144101+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11811","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STX4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"STX4","entity_type":"gene"},{"created":"2022-03-23T16:23:56.202359+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11811","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STXBP2 as ready","entity_name":"STXBP2","entity_type":"gene"},{"created":"2022-03-23T16:23:56.192206+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11811","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stxbp2 has been classified as Green List (High Evidence).","entity_name":"STXBP2","entity_type":"gene"},{"created":"2022-03-23T16:23:47.047791+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11811","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STXBP2 were changed from  to Haemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease 613101","entity_name":"STXBP2","entity_type":"gene"},{"created":"2022-03-23T16:23:18.727578+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11810","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STXBP2 were set to ","entity_name":"STXBP2","entity_type":"gene"},{"created":"2022-03-23T16:22:57.554593+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11809","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: STXBP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"STXBP2","entity_type":"gene"},{"created":"2022-03-23T16:22:36.415029+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11808","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STXBP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 19804848; Phenotypes: Haemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease 613101; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"STXBP2","entity_type":"gene"},{"created":"2022-03-23T16:18:17.444679+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11808","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SULT2B1 as ready","entity_name":"SULT2B1","entity_type":"gene"},{"created":"2022-03-23T16:18:17.431436+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11808","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sult2b1 has been classified as Green List (High Evidence).","entity_name":"SULT2B1","entity_type":"gene"},{"created":"2022-03-23T16:18:06.463273+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11808","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SULT2B1 were changed from  to Ichthyosis, congenital, autosomal recessive 14, MIM# 617571","entity_name":"SULT2B1","entity_type":"gene"},{"created":"2022-03-23T16:17:40.071210+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11807","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SULT2B1 were set to ","entity_name":"SULT2B1","entity_type":"gene"},{"created":"2022-03-23T16:17:15.546987+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11806","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SULT2B1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SULT2B1","entity_type":"gene"},{"created":"2022-03-23T16:16:55.809890+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11805","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SULT2B1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28575648; Phenotypes: Ichthyosis, congenital, autosomal recessive 14, MIM# 617571; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SULT2B1","entity_type":"gene"},{"created":"2022-03-23T16:13:22.072744+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11805","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SUMF1 as ready","entity_name":"SUMF1","entity_type":"gene"},{"created":"2022-03-23T16:13:22.060141+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11805","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sumf1 has been classified as Green List (High Evidence).","entity_name":"SUMF1","entity_type":"gene"},{"created":"2022-03-23T16:13:04.114011+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11805","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SUMF1 were changed from  to Multiple sulfatase deficiency (MIM#272200)","entity_name":"SUMF1","entity_type":"gene"},{"created":"2022-03-23T16:12:42.577458+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11804","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SUMF1 were set to ","entity_name":"SUMF1","entity_type":"gene"},{"created":"2022-03-23T16:10:50.844930+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11803","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SUMF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SUMF1","entity_type":"gene"},{"created":"2022-03-23T16:10:30.128455+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11802","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SUMF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17360554, 25885655, 28566233; Phenotypes: Multiple sulfatase deficiency (MIM#272200); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SUMF1","entity_type":"gene"},{"created":"2022-03-23T16:09:07.482275+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11802","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SUMO4 as ready","entity_name":"SUMO4","entity_type":"gene"},{"created":"2022-03-23T16:09:07.472625+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11802","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sumo4 has been classified as Red List (Low Evidence).","entity_name":"SUMO4","entity_type":"gene"},{"created":"2022-03-23T16:08:57.890808+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11802","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SUMO4 were changed from  to {Diabetes mellitus, insulin-dependent, 5} 600320","entity_name":"SUMO4","entity_type":"gene"},{"created":"2022-03-23T16:04:09.694257+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11801","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SUMO4 were set to ","entity_name":"SUMO4","entity_type":"gene"},{"created":"2022-03-23T16:03:46.578936+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11800","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SUMO4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SUMO4","entity_type":"gene"},{"created":"2022-03-23T15:59:39.074945+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11799","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SUMO4 as Red List (low evidence)","entity_name":"SUMO4","entity_type":"gene"},{"created":"2022-03-23T15:59:39.063881+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11799","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sumo4 has been classified as Red List (Low Evidence).","entity_name":"SUMO4","entity_type":"gene"},{"created":"2022-03-23T15:59:02.123603+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11798","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SUMO4: Rating: RED; Mode of pathogenicity: None; Publications: 15123604; Phenotypes: {Diabetes mellitus, insulin-dependent, 5} 600320; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SUMO4","entity_type":"gene"},{"created":"2022-03-23T15:57:24.570488+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11798","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SURF1 as ready","entity_name":"SURF1","entity_type":"gene"},{"created":"2022-03-23T15:57:24.559870+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11798","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: surf1 has been classified as Green List (High Evidence).","entity_name":"SURF1","entity_type":"gene"},{"created":"2022-03-23T15:57:17.005817+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11798","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SURF1 were changed from  to Charcot-Marie-Tooth disease, type 4K MIM#616684; Mitochondrial complex IV deficiency, nuclear type 1 MIM#220110","entity_name":"SURF1","entity_type":"gene"},{"created":"2022-03-23T15:56:52.073978+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11797","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SURF1 were set to ","entity_name":"SURF1","entity_type":"gene"},{"created":"2022-03-23T15:56:27.561075+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11796","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SURF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SURF1","entity_type":"gene"},{"created":"2022-03-23T15:56:06.453699+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11795","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association.; to: Well established gene-disease association with mitochondrial disease.","entity_name":"SURF1","entity_type":"gene"},{"created":"2022-03-23T15:55:49.188257+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11795","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SURF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 9843204, 9837813; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 1, MIM# 220110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SURF1","entity_type":"gene"},{"created":"2022-03-23T15:53:59.483391+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11795","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SUZ12 as ready","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:53:59.471314+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11795","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: suz12 has been classified as Green List (High Evidence).","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:53:52.042225+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11795","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SUZ12 were changed from  to Imagawa-Matsumoto syndrome, MIM# 618786","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:53:49.869372+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SUZ12 as ready","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:53:49.858586+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: suz12 has been classified as Green List (High Evidence).","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:53:43.419520+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SUZ12 were changed from  to Imagawa-Matsumoto syndrome, MIM# 618786","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:53:13.020731+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SUZ12 were set to ","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:52:44.450554+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SUZ12 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:52:22.663935+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.104","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SUZ12 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:52:07.346283+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11794","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SUZ12 were set to ","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:51:26.272603+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SUZ12: Rating: GREEN; Mode of pathogenicity: None; Publications: 31736240, 28229514; Phenotypes: Imagawa-Matsumoto syndrome, MIM# 618786; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:51:03.468528+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11793","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SUZ12 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:50:09.153665+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11792","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: More than 10 unrelated individuals reported.; to: More than 10 unrelated individuals reported, ID and overgrowth.","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T15:49:47.214390+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11792","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SUZ12: Rating: GREEN; Mode of pathogenicity: None; Publications: 31736240, 28229514; Phenotypes: Imagawa-Matsumoto syndrome, MIM# 618786; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SUZ12","entity_type":"gene"},{"created":"2022-03-23T14:07:16.909908+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11792","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NLGN3: Rating: ; Mode of pathogenicity: None; Publications: 28584888, 12669065, 25167861; Phenotypes: {Asperger syndrome susceptibility, X-linked 1} - MIM#300494, {Autism susceptibility, X-linked 1} - MIM#300425; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T14:07:13.161566+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4580","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NLGN3: Rating: GREEN; Mode of pathogenicity: None; Publications: 28584888, 12669065, 25167861; Phenotypes: {Asperger syndrome susceptibility, X-linked 1} - MIM#300494, {Autism susceptibility, X-linked 1} - MIM#300425; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T14:07:10.920188+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.175","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NLGN3: Rating: GREEN; Mode of pathogenicity: None; Publications: 28584888, 12669065, 25167861; Phenotypes: {Asperger syndrome susceptibility, X-linked 1} - MIM#300494, {Autism susceptibility, X-linked 1} - MIM#300425; Mode of inheritance: None","entity_name":"NLGN3","entity_type":"gene"},{"created":"2022-03-23T14:01:53.446218+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4580","user_name":"Elena Savva","item_type":"entity","text":"reviewed gene: KCND3: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 35021282, 32823520, 34067185, 34361012; Phenotypes: Spinocerebellar ataxia 19 MIM#607346; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","entity_name":"KCND3","entity_type":"gene"},{"created":"2022-03-23T13:16:07.183656+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11792","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NKX3-2: Rating: GREEN; Mode of pathogenicity: None; Publications: 20004766, 29704686; Phenotypes: Spondylo-megaepiphyseal-metaphyseal dysplasia - MIM#613330; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NKX3-2","entity_type":"gene"},{"created":"2022-03-23T13:15:58.570972+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.59","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NKX3-2: Rating: GREEN; Mode of pathogenicity: None; Publications: 20004766, 29704686; Phenotypes: Spondylo-megaepiphyseal-metaphyseal dysplasia (MIM#613330); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NKX3-2","entity_type":"gene"}]}