{"count":220489,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=84","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=82","results":[{"created":"2025-12-17T16:48:59.992748+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1375","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SDHC as ready","entity_name":"SDHC","entity_type":"gene"},{"created":"2025-12-17T16:48:59.981855+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1375","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sdhc has been classified as Red List (Low Evidence).","entity_name":"SDHC","entity_type":"gene"},{"created":"2025-12-17T16:48:53.176376+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1375","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SDHC: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SDHC","entity_type":"gene"},{"created":"2025-12-17T16:46:18.811653+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1375","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NUP62 as ready","entity_name":"NUP62","entity_type":"gene"},{"created":"2025-12-17T16:46:18.801472+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1375","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nup62 has been classified as Red List (Low Evidence).","entity_name":"NUP62","entity_type":"gene"},{"created":"2025-12-17T16:45:08.355172+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1375","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATPAF2 as ready","entity_name":"ATPAF2","entity_type":"gene"},{"created":"2025-12-17T16:45:08.344633+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1375","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atpaf2 has been classified as Red List (Low Evidence).","entity_name":"ATPAF2","entity_type":"gene"},{"created":"2025-12-17T16:45:04.714195+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1375","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ATPAF2 were changed from  to Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1, OMIM# 604273","entity_name":"ATPAF2","entity_type":"gene"},{"created":"2025-12-17T16:44:13.994479+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1374","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ATPAF2 were set to ","entity_name":"ATPAF2","entity_type":"gene"},{"created":"2025-12-17T16:43:34.315675+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1373","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ATPAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ATPAF2","entity_type":"gene"},{"created":"2025-12-17T16:36:50.857515+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1372","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WARS2 as ready","entity_name":"WARS2","entity_type":"gene"},{"created":"2025-12-17T16:36:50.847092+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1372","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wars2 has been classified as Green List (High Evidence).","entity_name":"WARS2","entity_type":"gene"},{"created":"2025-12-17T16:36:48.230406+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1372","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WARS2 were changed from  to Parkinsonism-dystonia 3, childhood-onset, MIM# 619738; Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures, MIM# 617710","entity_name":"WARS2","entity_type":"gene"},{"created":"2025-12-17T16:36:05.152912+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1371","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WARS2 were set to ","entity_name":"WARS2","entity_type":"gene"},{"created":"2025-12-17T16:35:29.505753+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1370","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WARS2","entity_type":"gene"},{"created":"2025-12-17T16:34:43.510216+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1369","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UQCC2 as ready","entity_name":"UQCC2","entity_type":"gene"},{"created":"2025-12-17T16:34:43.499281+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1369","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uqcc2 has been classified as Green List (High Evidence).","entity_name":"UQCC2","entity_type":"gene"},{"created":"2025-12-17T16:34:40.043923+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1369","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UQCC2 were changed from  to Mitochondrial complex III deficiency, nuclear type 7 - MIM#615824","entity_name":"UQCC2","entity_type":"gene"},{"created":"2025-12-17T16:33:59.202876+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1368","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UQCC2 were set to ","entity_name":"UQCC2","entity_type":"gene"},{"created":"2025-12-17T16:32:52.310218+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1367","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UQCC2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"UQCC2","entity_type":"gene"},{"created":"2025-12-17T16:31:37.493567+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1366","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC19 as ready","entity_name":"TTC19","entity_type":"gene"},{"created":"2025-12-17T16:31:37.482342+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1366","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc19 has been classified as Green List (High Evidence).","entity_name":"TTC19","entity_type":"gene"},{"created":"2025-12-17T16:31:26.059972+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1366","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC19 were changed from  to Mitochondrial complex III deficiency, nuclear type 2, MIM#615157","entity_name":"TTC19","entity_type":"gene"},{"created":"2025-12-17T16:30:50.329900+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1365","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC19 were set to ","entity_name":"TTC19","entity_type":"gene"},{"created":"2025-12-17T16:30:10.091057+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1364","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TTC19 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC19","entity_type":"gene"},{"created":"2025-12-17T16:27:19.938170+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1363","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSFM as ready","entity_name":"TSFM","entity_type":"gene"},{"created":"2025-12-17T16:27:19.927723+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1363","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tsfm has been classified as Green List (High Evidence).","entity_name":"TSFM","entity_type":"gene"},{"created":"2025-12-17T16:26:27.218704+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1363","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSFM were changed from  to Combined oxidative phosphorylation deficiency 3, MIM# 610505","entity_name":"TSFM","entity_type":"gene"},{"created":"2025-12-17T16:25:52.063802+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1362","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TSFM were set to ","entity_name":"TSFM","entity_type":"gene"},{"created":"2025-12-17T16:25:16.487281+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1361","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TSFM was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TSFM","entity_type":"gene"},{"created":"2025-12-17T16:23:28.607900+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1360","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRNT1 as ready","entity_name":"TRNT1","entity_type":"gene"},{"created":"2025-12-17T16:23:28.601002+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1360","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trnt1 has been classified as Green List (High Evidence).","entity_name":"TRNT1","entity_type":"gene"},{"created":"2025-12-17T16:23:25.721960+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1360","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRNT1 were changed from  to Retinitis pigmentosa and erythrocytic microcytosis, MIM# 616959; Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay, MIM# 616084","entity_name":"TRNT1","entity_type":"gene"},{"created":"2025-12-17T16:22:46.841693+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1359","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRNT1 were set to 25193871; 23553769; 29170023; 27389523; 26494905","entity_name":"TRNT1","entity_type":"gene"},{"created":"2025-12-17T16:22:17.881796+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1359","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRNT1 were set to ","entity_name":"TRNT1","entity_type":"gene"},{"created":"2025-12-17T16:21:21.307419+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1358","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRNT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRNT1","entity_type":"gene"},{"created":"2025-12-17T16:17:48.893799+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1357","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRMU as ready","entity_name":"TRMU","entity_type":"gene"},{"created":"2025-12-17T16:17:48.860785+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1357","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trmu has been classified as Green List (High Evidence).","entity_name":"TRMU","entity_type":"gene"},{"created":"2025-12-17T16:17:20.966822+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1357","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRMU were changed from  to Liver failure, transient infantile, MIM# 613070","entity_name":"TRMU","entity_type":"gene"},{"created":"2025-12-17T16:16:37.067461+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1356","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRMU were set to 19732863","entity_name":"TRMU","entity_type":"gene"},{"created":"2025-12-17T16:16:03.754618+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1355","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRMU were set to ","entity_name":"TRMU","entity_type":"gene"},{"created":"2025-12-17T16:15:16.996762+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1354","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRMU was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMU","entity_type":"gene"},{"created":"2025-12-17T16:14:43.743682+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1353","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRMU was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMU","entity_type":"gene"},{"created":"2025-12-17T16:13:50.712711+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1352","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRMT10C as ready","entity_name":"TRMT10C","entity_type":"gene"},{"created":"2025-12-17T16:13:50.706140+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1352","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trmt10c has been classified as Green List (High Evidence).","entity_name":"TRMT10C","entity_type":"gene"},{"created":"2025-12-17T16:13:45.424549+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1352","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRMT10C were changed from Combined oxidative phosphorylation deficiency 30, MIM# 616974 to Combined oxidative phosphorylation deficiency 30, MIM# 616974","entity_name":"TRMT10C","entity_type":"gene"},{"created":"2025-12-17T16:13:14.456319+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1351","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRMT10C were changed from  to Combined oxidative phosphorylation deficiency 30, MIM# 616974","entity_name":"TRMT10C","entity_type":"gene"},{"created":"2025-12-17T16:12:23.503390+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1350","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRMT10C were set to 27132592; 33886802","entity_name":"TRMT10C","entity_type":"gene"},{"created":"2025-12-17T16:11:45.608765+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1349","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRMT10C were set to ","entity_name":"TRMT10C","entity_type":"gene"},{"created":"2025-12-17T16:10:50.471859+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1348","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRIT1 as ready","entity_name":"TRIT1","entity_type":"gene"},{"created":"2025-12-17T16:10:50.460604+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1348","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trit1 has been classified as Green List (High Evidence).","entity_name":"TRIT1","entity_type":"gene"},{"created":"2025-12-17T16:10:29.685251+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1348","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TPK1 as ready","entity_name":"TPK1","entity_type":"gene"},{"created":"2025-12-17T16:10:29.677756+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1348","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tpk1 has been classified as Green List (High Evidence).","entity_name":"TPK1","entity_type":"gene"},{"created":"2025-12-17T09:59:47.947838+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1348","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TPK1 were changed from  to Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type), MIM# 614458","entity_name":"TPK1","entity_type":"gene"},{"created":"2025-12-17T09:59:14.420742+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1347","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TPK1 were set to ","entity_name":"TPK1","entity_type":"gene"},{"created":"2025-12-17T09:58:33.273103+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1346","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TPK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TPK1","entity_type":"gene"},{"created":"2025-12-17T09:57:48.150921+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1345","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM70 as ready","entity_name":"TMEM70","entity_type":"gene"},{"created":"2025-12-17T09:57:48.141022+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1345","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem70 has been classified as Green List (High Evidence).","entity_name":"TMEM70","entity_type":"gene"},{"created":"2025-12-17T09:57:45.341872+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1345","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM70 were changed from  to Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2, MIM# 614052","entity_name":"TMEM70","entity_type":"gene"},{"created":"2025-12-17T09:57:07.837185+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1344","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM70 were set to ","entity_name":"TMEM70","entity_type":"gene"},{"created":"2025-12-17T09:56:31.029959+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1343","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMEM70 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM70","entity_type":"gene"},{"created":"2025-12-17T09:55:41.748554+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1342","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TIMM8A as ready","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2025-12-17T09:55:41.740866+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1342","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: timm8a has been classified as Green List (High Evidence).","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2025-12-17T09:55:38.416624+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1342","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TIMM8A were changed from  to Mohr-Tranebjaerg syndrome, MIM# 304700","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2025-12-17T09:55:04.193596+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1341","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TIMM8A were set to ","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2025-12-17T09:54:11.281027+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1340","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TIMM8A was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2025-12-17T09:53:32.391821+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1339","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Progressive syndrome that includes deafness, visual disability leading to cortical blindness, dystonia, fractures, and intellectual impairment.; to: Progressive syndrome that includes deafness, visual disability leading to cortical blindness, dystonia, fractures, and intellectual impairment.\r\n\r\nComponent of the inner mitochondrial membrane.","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2025-12-17T09:52:32.621593+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1339","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SURF1 as ready","entity_name":"SURF1","entity_type":"gene"},{"created":"2025-12-17T09:52:32.610721+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1339","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":"2025-12-17T09:52:29.554023+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1339","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":"2025-12-17T09:51:41.760226+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1338","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SURF1 were set to ","entity_name":"SURF1","entity_type":"gene"},{"created":"2025-12-17T09:51:02.962007+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1337","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":"2025-12-17T09:50:18.727459+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1336","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SUCLG1 as ready","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2025-12-17T09:50:18.720707+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1336","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: suclg1 has been classified as Green List (High Evidence).","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2025-12-17T09:50:12.648944+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1336","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SUCLG1 were changed from  to Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) MIM#245400","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2025-12-17T09:49:48.823409+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.294","user_name":"Sarah Milton","item_type":"entity","text":"reviewed Region: ISCA-37423-Gain: Rating: ; Mode of pathogenicity: None; Publications: PMID: 23345203; Phenotypes: ; Mode of inheritance: None","entity_name":"ISCA-37423-Gain","entity_type":"region"},{"created":"2025-12-17T09:49:36.967524+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1335","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SUCLG1 were set to ","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2025-12-17T09:48:54.985055+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1334","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SUCLG1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SUCLG1","entity_type":"gene"},{"created":"2025-12-17T09:48:12.288469+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1333","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SUCLA2 as ready","entity_name":"SUCLA2","entity_type":"gene"},{"created":"2025-12-17T09:48:12.277919+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1333","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sucla2 has been classified as Green List (High Evidence).","entity_name":"SUCLA2","entity_type":"gene"},{"created":"2025-12-17T09:48:09.045847+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1333","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SUCLA2 were changed from  to Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria), MIM# 612073, MONDO:0012791","entity_name":"SUCLA2","entity_type":"gene"},{"created":"2025-12-17T09:47:30.827483+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1332","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SUCLA2 were set to ","entity_name":"SUCLA2","entity_type":"gene"},{"created":"2025-12-17T09:46:55.943395+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1331","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SUCLA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SUCLA2","entity_type":"gene"},{"created":"2025-12-17T09:46:01.966717+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1330","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC25A19 as ready","entity_name":"SLC25A19","entity_type":"gene"},{"created":"2025-12-17T09:46:01.956140+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1330","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc25a19 has been classified as Green List (High Evidence).","entity_name":"SLC25A19","entity_type":"gene"},{"created":"2025-12-17T09:45:59.046274+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1330","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC25A19 were changed from  to Microcephaly, Amish type, MIM#607196; Thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type), MIM#613710","entity_name":"SLC25A19","entity_type":"gene"},{"created":"2025-12-17T09:45:22.424689+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1329","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC25A19 were set to ","entity_name":"SLC25A19","entity_type":"gene"},{"created":"2025-12-17T09:44:38.015875+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1328","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC25A19 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC25A19","entity_type":"gene"},{"created":"2025-12-17T09:43:45.293701+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1327","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC25A1 as ready","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2025-12-17T09:43:45.283803+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1327","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc25a1 has been classified as Green List (High Evidence).","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2025-12-17T09:43:42.629085+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1327","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC25A1 were changed from  to Combined D-2- and L-2-hydroxyglutaric aciduria MIM#: 615182, MONDO:0014072; Myasthenic syndrome, congenital, 23, presynaptic, MIM#618197, MONDO:0032596","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2025-12-17T09:43:06.068374+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1326","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC25A1 were set to 26870663; 31527857; 31808147; 23561848; 23393310","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2025-12-17T09:42:40.401633+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1325","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC25A1 were set to ","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2025-12-17T09:42:32.717533+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.510","user_name":"Sarah Milton","item_type":"panel","text":"Copied Region ISCA-37423-Gain from panel Common deletion and duplication syndromes","entity_name":null,"entity_type":null},{"created":"2025-12-17T09:42:29.540400+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.510","user_name":"Sarah Milton","item_type":"entity","text":"Region: ISCA-37423-Gain was added\nRegion: ISCA-37423-Gain was added to Intellectual disability syndromic and non-syndromic. Sources: Expert Review Green,Expert list\nSV/CNV tags were added to Region: ISCA-37423-Gain.\nMode of inheritance for Region: ISCA-37423-Gain was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for Region: ISCA-37423-Gain were set to 26097203; 25520754\nPhenotypes for Region: ISCA-37423-Gain were set to 8p23.1 duplication syndrome; intellectual disability; congenital heart disease","entity_name":"ISCA-37423-Gain","entity_type":"region"},{"created":"2025-12-17T09:41:47.059114+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.512","user_name":"Sarah Milton","item_type":"panel","text":"Copied Region ISCA-37423-Gain from panel Common deletion and duplication syndromes","entity_name":null,"entity_type":null},{"created":"2025-12-17T09:41:46.877377+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1324","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC25A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2025-12-17T09:41:46.872219+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.512","user_name":"Sarah Milton","item_type":"entity","text":"Region: ISCA-37423-Gain was added\nRegion: ISCA-37423-Gain was added to Congenital Heart Defect. Sources: Expert Review Green,Expert list\nSV/CNV tags were added to Region: ISCA-37423-Gain.\nMode of inheritance for Region: ISCA-37423-Gain was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for Region: ISCA-37423-Gain were set to 26097203; 25520754\nPhenotypes for Region: ISCA-37423-Gain were set to 8p23.1 duplication syndrome; intellectual disability; congenital heart disease","entity_name":"ISCA-37423-Gain","entity_type":"region"},{"created":"2025-12-17T09:41:09.528353+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.1323","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC25A1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2025-12-17T09:41:06.221275+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.294","user_name":"Sarah Milton","item_type":"panel","text":"Copied Region ISCA-37423-Gain from panel Common deletion and duplication syndromes","entity_name":null,"entity_type":null}]}