{"count":220497,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=99","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=97","results":[{"created":"2025-12-07T13:03:25.876606+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.300","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37393-Gain as ready","entity_name":"ISCA-37393-Gain","entity_type":"region"},{"created":"2025-12-07T13:03:25.865657+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.300","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37393-gain has been classified as Green List (High Evidence).","entity_name":"ISCA-37393-Gain","entity_type":"region"},{"created":"2025-12-07T13:03:06.837259+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.479","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37393-Gain as ready","entity_name":"ISCA-37393-Gain","entity_type":"region"},{"created":"2025-12-07T13:03:06.813559+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.479","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37393-gain has been classified as Green List (High Evidence).","entity_name":"ISCA-37393-Gain","entity_type":"region"},{"created":"2025-12-07T13:02:42.962161+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37393-Gain as ready","entity_name":"ISCA-37393-Gain","entity_type":"region"},{"created":"2025-12-07T13:02:42.952633+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37393-gain has been classified as Green List (High Evidence).","entity_name":"ISCA-37393-Gain","entity_type":"region"},{"created":"2025-12-07T13:02:22.290188+11:00","panel_name":"Hand and foot malformations","panel_id":3729,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37394-Loss as ready","entity_name":"ISCA-37394-Loss","entity_type":"region"},{"created":"2025-12-07T13:02:22.266971+11:00","panel_name":"Hand and foot malformations","panel_id":3729,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37394-loss has been classified as Green List (High Evidence).","entity_name":"ISCA-37394-Loss","entity_type":"region"},{"created":"2025-12-07T13:01:54.542991+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37394-Loss as ready","entity_name":"ISCA-37394-Loss","entity_type":"region"},{"created":"2025-12-07T13:01:54.532624+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37394-loss has been classified as Green List (High Evidence).","entity_name":"ISCA-37394-Loss","entity_type":"region"},{"created":"2025-12-06T19:56:10.185856+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37396-Loss as ready","entity_name":"ISCA-37396-Loss","entity_type":"region"},{"created":"2025-12-06T19:56:10.176566+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37396-loss has been classified as Green List (High Evidence).","entity_name":"ISCA-37396-Loss","entity_type":"region"},{"created":"2025-12-06T19:55:53.354564+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.374","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37396-Loss as ready","entity_name":"ISCA-37396-Loss","entity_type":"region"},{"created":"2025-12-06T19:55:53.347964+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.374","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37396-loss has been classified as Green List (High Evidence).","entity_name":"ISCA-37396-Loss","entity_type":"region"},{"created":"2025-12-06T19:55:38.161710+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37397-Gain as ready","entity_name":"ISCA-37397-Gain","entity_type":"region"},{"created":"2025-12-06T19:55:38.152493+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37397-gain has been classified as Green List (High Evidence).","entity_name":"ISCA-37397-Gain","entity_type":"region"},{"created":"2025-12-06T19:55:22.708304+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.509","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37397-Loss as ready","entity_name":"ISCA-37397-Loss","entity_type":"region"},{"created":"2025-12-06T19:55:22.702047+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.509","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37397-loss has been classified as Green List (High Evidence).","entity_name":"ISCA-37397-Loss","entity_type":"region"},{"created":"2025-12-06T19:55:09.473142+11:00","panel_name":"Growth failure","panel_id":3631,"panel_version":"1.86","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37397-Loss as ready","entity_name":"ISCA-37397-Loss","entity_type":"region"},{"created":"2025-12-06T19:55:09.464857+11:00","panel_name":"Growth failure","panel_id":3631,"panel_version":"1.86","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37397-loss has been classified as Green List (High Evidence).","entity_name":"ISCA-37397-Loss","entity_type":"region"},{"created":"2025-12-06T19:54:53.182148+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37397-Loss as ready","entity_name":"ISCA-37397-Loss","entity_type":"region"},{"created":"2025-12-06T19:54:53.173356+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37397-loss has been classified as Green List (High Evidence).","entity_name":"ISCA-37397-Loss","entity_type":"region"},{"created":"2025-12-06T19:54:37.430793+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37400-Gain as ready","entity_name":"ISCA-37400-Gain","entity_type":"region"},{"created":"2025-12-06T19:54:37.421525+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37400-gain has been classified as Green List (High Evidence).","entity_name":"ISCA-37400-Gain","entity_type":"region"},{"created":"2025-12-06T19:54:21.333613+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.233","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37400-Loss as ready","entity_name":"ISCA-37400-Loss","entity_type":"region"},{"created":"2025-12-06T19:54:21.327564+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.233","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37400-loss has been classified as Green List (High Evidence).","entity_name":"ISCA-37400-Loss","entity_type":"region"},{"created":"2025-12-06T19:53:58.912110+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.303","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37400-Loss as ready","entity_name":"ISCA-37400-Loss","entity_type":"region"},{"created":"2025-12-06T19:53:58.903384+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.303","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37400-loss has been classified as Green List (High Evidence).","entity_name":"ISCA-37400-Loss","entity_type":"region"},{"created":"2025-12-06T19:53:44.292141+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37400-Loss as ready","entity_name":"ISCA-37400-Loss","entity_type":"region"},{"created":"2025-12-06T19:53:44.283253+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37400-loss has been classified as Green List (High Evidence).","entity_name":"ISCA-37400-Loss","entity_type":"region"},{"created":"2025-12-06T19:53:30.515708+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.233","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37404-Gain as ready","entity_name":"ISCA-37404-Gain","entity_type":"region"},{"created":"2025-12-06T19:53:30.506872+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.233","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37404-gain has been classified as Green List (High Evidence).","entity_name":"ISCA-37404-Gain","entity_type":"region"},{"created":"2025-12-06T19:53:09.836977+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked Region: ISCA-37404-Gain as ready","entity_name":"ISCA-37404-Gain","entity_type":"region"},{"created":"2025-12-06T19:53:09.827702+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.486","user_name":"Zornitza Stark","item_type":"entity","text":"Region: isca-37404-gain has been classified as Green List (High Evidence).","entity_name":"ISCA-37404-Gain","entity_type":"region"},{"created":"2025-12-06T17:21:44.465762+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1212","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRPPRC as ready","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2025-12-06T17:21:44.452226+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1212","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":"2025-12-06T17:21:40.584594+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1212","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRPPRC were changed from  to Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian) MIM#220111","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2025-12-06T17:21:03.263718+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1211","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LRPPRC were set to ","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2025-12-06T14:43:14.931067+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1210","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LRPPRC was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2025-12-06T14:42:27.687971+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1209","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LIPT2 as ready","entity_name":"LIPT2","entity_type":"gene"},{"created":"2025-12-06T14:42:27.678155+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1209","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lipt2 has been classified as Green List (High Evidence).","entity_name":"LIPT2","entity_type":"gene"},{"created":"2025-12-06T14:42:24.852726+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1209","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LIPT2 were changed from  to Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities, MIM# 617668","entity_name":"LIPT2","entity_type":"gene"},{"created":"2025-12-06T14:41:47.603228+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1208","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LIPT2 were set to ","entity_name":"LIPT2","entity_type":"gene"},{"created":"2025-12-06T14:41:06.822142+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1207","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LIPT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LIPT2","entity_type":"gene"},{"created":"2025-12-06T14:40:24.833688+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1206","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LIAS as ready","entity_name":"LIAS","entity_type":"gene"},{"created":"2025-12-06T14:40:24.823522+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1206","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lias has been classified as Green List (High Evidence).","entity_name":"LIAS","entity_type":"gene"},{"created":"2025-12-06T14:40:21.618306+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1206","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LIAS were changed from  to Hyperglycinaemia, lactic acidosis, and seizures, MIM# 614462","entity_name":"LIAS","entity_type":"gene"},{"created":"2025-12-06T14:39:51.513360+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1205","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LIAS were set to ","entity_name":"LIAS","entity_type":"gene"},{"created":"2025-12-06T14:38:45.723572+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1204","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LIAS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LIAS","entity_type":"gene"},{"created":"2025-12-06T14:38:07.660228+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1203","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LARS2 as ready","entity_name":"LARS2","entity_type":"gene"},{"created":"2025-12-06T14:38:07.650459+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1203","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lars2 has been classified as Green List (High Evidence).","entity_name":"LARS2","entity_type":"gene"},{"created":"2025-12-06T14:38:04.541240+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1203","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LARS2 were changed from  to Perrault syndrome 4; Hydrops, lactic acidosis, and sideroblastic anaemia, MIM# 617021; Leukodystrophy","entity_name":"LARS2","entity_type":"gene"},{"created":"2025-12-06T14:37:21.755741+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1202","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LARS2 were set to ","entity_name":"LARS2","entity_type":"gene"},{"created":"2025-12-06T14:36:44.693742+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1201","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARS2","entity_type":"gene"},{"created":"2025-12-06T14:35:59.973503+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1200","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ISCU as ready","entity_name":"ISCU","entity_type":"gene"},{"created":"2025-12-06T14:35:59.963002+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1200","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iscu has been classified as Green List (High Evidence).","entity_name":"ISCU","entity_type":"gene"},{"created":"2025-12-06T14:35:57.309292+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1200","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ISCU were changed from  to Myopathy with lactic acidosis, hereditary, MIM# 255125","entity_name":"ISCU","entity_type":"gene"},{"created":"2025-12-06T14:35:23.835805+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1199","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ISCU were set to ","entity_name":"ISCU","entity_type":"gene"},{"created":"2025-12-06T14:34:54.717870+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1198","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ISCU was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ISCU","entity_type":"gene"},{"created":"2025-12-06T14:34:13.819052+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1197","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IARS2 as ready","entity_name":"IARS2","entity_type":"gene"},{"created":"2025-12-06T14:34:13.809247+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1197","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iars2 has been classified as Green List (High Evidence).","entity_name":"IARS2","entity_type":"gene"},{"created":"2025-12-06T14:34:08.779790+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1197","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IARS2 were changed from  to Cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia, MIM# 616007","entity_name":"IARS2","entity_type":"gene"},{"created":"2025-12-06T14:33:40.101453+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1196","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IARS2 were set to ","entity_name":"IARS2","entity_type":"gene"},{"created":"2025-12-06T14:33:09.318031+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1195","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IARS2","entity_type":"gene"},{"created":"2025-12-06T14:32:26.727948+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1194","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSD17B10 as ready","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2025-12-06T14:32:26.718090+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1194","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hsd17b10 has been classified as Green List (High Evidence).","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2025-12-06T14:32:24.006820+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1194","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSD17B10 were changed from  to HSD10 mitochondrial disease, MIM# 300438","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2025-12-06T14:31:45.635659+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1193","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HSD17B10 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2025-12-06T14:31:02.856932+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1192","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSPD1 as ready","entity_name":"HSPD1","entity_type":"gene"},{"created":"2025-12-06T14:31:02.849413+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1192","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hspd1 has been classified as Green List (High Evidence).","entity_name":"HSPD1","entity_type":"gene"},{"created":"2025-12-06T14:31:00.240928+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1192","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSPD1 were changed from  to Leukodystrophy, hypomyelinating, 4, MIM# 612233; Spastic paraplegia 13, autosomal dominant, MIM# 605280","entity_name":"HSPD1","entity_type":"gene"},{"created":"2025-12-06T14:30:29.439756+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1191","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HSPD1 were set to ","entity_name":"HSPD1","entity_type":"gene"},{"created":"2025-12-06T14:30:00.975942+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1190","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HSPD1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"HSPD1","entity_type":"gene"},{"created":"2025-12-05T23:17:54.815902+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1189","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HIBCH as ready","entity_name":"HIBCH","entity_type":"gene"},{"created":"2025-12-05T23:17:54.808578+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1189","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hibch has been classified as Green List (High Evidence).","entity_name":"HIBCH","entity_type":"gene"},{"created":"2025-12-05T23:17:50.899896+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1189","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HIBCH were changed from  to 3-hydroxyisobutryl-CoA hydrolase deficiency, MIM# 250620","entity_name":"HIBCH","entity_type":"gene"},{"created":"2025-12-05T23:14:54.841688+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1188","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HIBCH were set to 26026795; 25251209; 24299452; 32677093","entity_name":"HIBCH","entity_type":"gene"},{"created":"2025-12-05T18:33:49.770981+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1187","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HIBCH were set to ","entity_name":"HIBCH","entity_type":"gene"},{"created":"2025-12-05T18:33:14.929479+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1186","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HIBCH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HIBCH","entity_type":"gene"},{"created":"2025-12-05T18:32:36.304219+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1185","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HCCS as ready","entity_name":"HCCS","entity_type":"gene"},{"created":"2025-12-05T18:32:36.293289+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1185","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hccs has been classified as Green List (High Evidence).","entity_name":"HCCS","entity_type":"gene"},{"created":"2025-12-05T18:32:33.609264+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1185","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HCCS were changed from  to Linear skin defects with multiple congenital anomalies 1, MIM# 309801","entity_name":"HCCS","entity_type":"gene"},{"created":"2025-12-05T18:31:52.742152+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1184","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HCCS were set to ","entity_name":"HCCS","entity_type":"gene"},{"created":"2025-12-05T18:30:43.219671+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1183","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HCCS was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HCCS","entity_type":"gene"},{"created":"2025-12-05T18:29:54.354579+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1182","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GLRX5 as ready","entity_name":"GLRX5","entity_type":"gene"},{"created":"2025-12-05T18:29:54.346988+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1182","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: glrx5 has been classified as Green List (High Evidence).","entity_name":"GLRX5","entity_type":"gene"},{"created":"2025-12-05T18:29:51.194130+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1182","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GLRX5 were changed from  to Anaemia, sideroblastic, 3, pyridoxine-refractory, MIM# 616860","entity_name":"GLRX5","entity_type":"gene"},{"created":"2025-12-05T18:29:00.973769+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1181","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GLRX5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GLRX5","entity_type":"gene"},{"created":"2025-12-05T18:28:21.359482+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1180","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GFM1 as ready","entity_name":"GFM1","entity_type":"gene"},{"created":"2025-12-05T18:28:21.351873+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1180","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gfm1 has been classified as Green List (High Evidence).","entity_name":"GFM1","entity_type":"gene"},{"created":"2025-12-05T18:28:09.528996+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1180","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GFM1 were changed from  to Combined oxidative phosphorylation deficiency 1 MIM#609060","entity_name":"GFM1","entity_type":"gene"},{"created":"2025-12-05T18:27:40.523497+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1179","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GFM1 were set to ","entity_name":"GFM1","entity_type":"gene"},{"created":"2025-12-05T18:27:11.753786+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1178","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GFM1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GFM1","entity_type":"gene"},{"created":"2025-12-05T18:26:22.223511+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1177","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLAD1 as ready","entity_name":"FLAD1","entity_type":"gene"},{"created":"2025-12-05T18:26:22.213166+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1177","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flad1 has been classified as Green List (High Evidence).","entity_name":"FLAD1","entity_type":"gene"},{"created":"2025-12-05T18:26:18.992707+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1177","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLAD1 were changed from  to Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency MIM#255100","entity_name":"FLAD1","entity_type":"gene"},{"created":"2025-12-05T18:25:35.688767+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1176","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLAD1 were set to ","entity_name":"FLAD1","entity_type":"gene"},{"created":"2025-12-05T18:24:55.808132+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1175","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FLAD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FLAD1","entity_type":"gene"},{"created":"2025-12-05T18:24:10.775220+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1174","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ETHE1 as ready","entity_name":"ETHE1","entity_type":"gene"},{"created":"2025-12-05T18:24:10.768008+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1174","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ethe1 has been classified as Green List (High Evidence).","entity_name":"ETHE1","entity_type":"gene"}]}