{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=280","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=278","results":[{"created":"2025-03-24T17:25:52.983363+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1783","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC7A were set to ","entity_name":"TTC7A","entity_type":"gene"},{"created":"2025-03-24T17:24:30.051476+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1782","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC37 as ready","entity_name":"TTC37","entity_type":"gene"},{"created":"2025-03-24T17:24:30.043910+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1782","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc37 has been classified as Green List (High Evidence).","entity_name":"TTC37","entity_type":"gene"},{"created":"2025-03-24T17:24:24.969625+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1782","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC37 were changed from Trichohepatoenteric syndrome 1, 222470 (3) to Trichohepatoenteric syndrome 1 MIM#222470","entity_name":"TTC37","entity_type":"gene"},{"created":"2025-03-24T17:24:14.203713+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1781","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC37 were set to ","entity_name":"TTC37","entity_type":"gene"},{"created":"2025-03-24T17:19:58.930155+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1780","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM237 as ready","entity_name":"TMEM237","entity_type":"gene"},{"created":"2025-03-24T17:19:58.920470+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1780","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem237 has been classified as Green List (High Evidence).","entity_name":"TMEM237","entity_type":"gene"},{"created":"2025-03-24T17:19:54.792228+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1780","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM237 were changed from Joubert syndrome 14, 614424 (3) to Joubert syndrome 14, MIM#614424","entity_name":"TMEM237","entity_type":"gene"},{"created":"2025-03-24T17:19:43.932165+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1779","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM237 were set to ","entity_name":"TMEM237","entity_type":"gene"},{"created":"2025-03-24T17:19:17.810262+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1778","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM231 as ready","entity_name":"TMEM231","entity_type":"gene"},{"created":"2025-03-24T17:19:17.803526+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1778","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem231 has been classified as Green List (High Evidence).","entity_name":"TMEM231","entity_type":"gene"},{"created":"2025-03-24T17:19:14.738632+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1778","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM231 were changed from Joubert syndrome 20, 614970 (3) to Joubert syndrome 20, MIM#614970; Meckel syndrome 11, MIM#615397","entity_name":"TMEM231","entity_type":"gene"},{"created":"2025-03-24T17:18:53.125425+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1777","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM231 were set to ","entity_name":"TMEM231","entity_type":"gene"},{"created":"2025-03-24T17:18:27.740053+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1776","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM165 as ready","entity_name":"TMEM165","entity_type":"gene"},{"created":"2025-03-24T17:18:27.732041+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1776","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem165 has been classified as Green List (High Evidence).","entity_name":"TMEM165","entity_type":"gene"},{"created":"2025-03-24T17:18:24.738473+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1776","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM165 were changed from Congenital disorder of glycosylation, type IIk, 614727 (3) to Congenital disorder of glycosylation, type IIk, MIM#614727","entity_name":"TMEM165","entity_type":"gene"},{"created":"2025-03-24T17:18:13.751497+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1775","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM165 were set to ","entity_name":"TMEM165","entity_type":"gene"},{"created":"2025-03-24T17:17:38.704385+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1774","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TJP2 as ready","entity_name":"TJP2","entity_type":"gene"},{"created":"2025-03-24T17:17:38.697508+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1774","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tjp2 has been classified as Green List (High Evidence).","entity_name":"TJP2","entity_type":"gene"},{"created":"2025-03-24T17:17:36.126320+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1774","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TJP2 were changed from Cholestasis, progressive familial intrahepatic 4, 615878 (3) to Cholestasis, progressive familial intrahepatic 4, MIM# 615878","entity_name":"TJP2","entity_type":"gene"},{"created":"2025-03-24T17:17:25.164723+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1773","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TJP2 were set to ","entity_name":"TJP2","entity_type":"gene"},{"created":"2025-03-24T17:16:53.672174+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1772","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCN2 as ready","entity_name":"TCN2","entity_type":"gene"},{"created":"2025-03-24T17:16:53.665404+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1772","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tcn2 has been classified as Green List (High Evidence).","entity_name":"TCN2","entity_type":"gene"},{"created":"2025-03-24T17:16:51.111014+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1772","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TCN2 were changed from Transcobalamin II deficiency, 275350 (3) to Transcobalamin II deficiency MIM#275350","entity_name":"TCN2","entity_type":"gene"},{"created":"2025-03-24T17:16:39.983348+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1771","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCN2 were set to ","entity_name":"TCN2","entity_type":"gene"},{"created":"2025-03-24T17:15:59.265830+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1770","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBX19 as ready","entity_name":"TBX19","entity_type":"gene"},{"created":"2025-03-24T17:15:59.257673+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1770","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbx19 has been classified as Green List (High Evidence).","entity_name":"TBX19","entity_type":"gene"},{"created":"2025-03-24T17:15:56.326670+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1770","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBX19 were changed from Adrenocorticotropic hormone deficiency, 201400 (3) to Adrenocorticotropic hormone deficiency, MIM# 201400","entity_name":"TBX19","entity_type":"gene"},{"created":"2025-03-24T17:15:45.319919+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1769","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBX19 were set to ","entity_name":"TBX19","entity_type":"gene"},{"created":"2025-03-24T17:15:17.906460+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1768","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBCK as ready","entity_name":"TBCK","entity_type":"gene"},{"created":"2025-03-24T17:15:17.900394+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1768","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbck has been classified as Green List (High Evidence).","entity_name":"TBCK","entity_type":"gene"},{"created":"2025-03-24T17:15:15.140697+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1768","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBCK were changed from Hypotonia, infantile, with psychomotor retardation and characteristic facies 3, 616900 (3), Autosomal recessive to Hypotonia, infantile, with psychomotor retardation and characteristic facies 3, MIM# 616900","entity_name":"TBCK","entity_type":"gene"},{"created":"2025-03-24T17:14:54.917751+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1767","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBCK were set to ","entity_name":"TBCK","entity_type":"gene"},{"created":"2025-03-24T17:14:07.822821+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1766","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STRADA as ready","entity_name":"STRADA","entity_type":"gene"},{"created":"2025-03-24T17:14:07.814995+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1766","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: strada has been classified as Green List (High Evidence).","entity_name":"STRADA","entity_type":"gene"},{"created":"2025-03-24T17:14:04.891823+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1766","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STRADA were changed from Polyhydramnios, megalencephaly, and symptomatic epilepsy, 611087 (3), Autosomal recessive to Polyhydramnios, megalencephaly, and symptomatic epilepsy MIM#611087","entity_name":"STRADA","entity_type":"gene"},{"created":"2025-03-24T17:13:53.858444+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1765","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STRADA were set to ","entity_name":"STRADA","entity_type":"gene"},{"created":"2025-03-24T17:13:10.456873+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1764","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STAT1 as ready","entity_name":"STAT1","entity_type":"gene"},{"created":"2025-03-24T17:13:10.449858+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1764","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stat1 has been classified as Green List (High Evidence).","entity_name":"STAT1","entity_type":"gene"},{"created":"2025-03-24T17:13:06.660911+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1764","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STAT1 were changed from Immunodeficiency 31B, mycobacterial and viral infections, autosomal recessive, 613796 (3) to Immunodeficiency 31B, mycobacterial and viral infections, autosomal recessive MIM#613796; Immunodeficiency 31B MONDO:0013427","entity_name":"STAT1","entity_type":"gene"},{"created":"2025-03-24T17:12:55.240446+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1763","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STAT1 were set to ","entity_name":"STAT1","entity_type":"gene"},{"created":"2025-03-24T17:12:31.144986+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1762","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ST3GAL5 as ready","entity_name":"ST3GAL5","entity_type":"gene"},{"created":"2025-03-24T17:12:31.138649+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1762","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: st3gal5 has been classified as Green List (High Evidence).","entity_name":"ST3GAL5","entity_type":"gene"},{"created":"2025-03-24T17:12:28.343721+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1762","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ST3GAL5 were changed from Salt and pepper developmental regression syndrome, 609056 (3), Autosomal recessive to Salt and pepper developmental regression syndrome, MIM# 609056","entity_name":"ST3GAL5","entity_type":"gene"},{"created":"2025-03-24T17:12:16.553508+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1761","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ST3GAL5 were set to ","entity_name":"ST3GAL5","entity_type":"gene"},{"created":"2025-03-24T17:11:53.353587+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1760","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SSR4 as ready","entity_name":"SSR4","entity_type":"gene"},{"created":"2025-03-24T17:11:53.347134+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1760","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ssr4 has been classified as Green List (High Evidence).","entity_name":"SSR4","entity_type":"gene"},{"created":"2025-03-24T17:11:51.142624+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1760","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SSR4 were changed from Congenital disorder of glycosylation, type Iy, 300934 (3), X-linked recessive to Congenital disorder of glycosylation, type Iy MIM#300934","entity_name":"SSR4","entity_type":"gene"},{"created":"2025-03-24T17:11:37.606615+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1759","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SSR4 were set to ","entity_name":"SSR4","entity_type":"gene"},{"created":"2025-03-24T17:11:10.512863+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1758","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SPINT2 as ready","entity_name":"SPINT2","entity_type":"gene"},{"created":"2025-03-24T17:11:10.504631+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1758","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spint2 has been classified as Green List (High Evidence).","entity_name":"SPINT2","entity_type":"gene"},{"created":"2025-03-24T17:11:07.768334+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1758","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SPINT2 were changed from Diarrhea 3, secretory sodium, congenital, syndromic, 270420 (3) to Diarrhoea 3, secretory sodium, congenital, syndromic, MIM#270420","entity_name":"SPINT2","entity_type":"gene"},{"created":"2025-03-24T17:10:46.860732+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1757","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SPINT2 were set to ","entity_name":"SPINT2","entity_type":"gene"},{"created":"2025-03-24T17:10:21.570682+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1756","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SPATA5 as ready","entity_name":"SPATA5","entity_type":"gene"},{"created":"2025-03-24T17:10:21.564498+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1756","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spata5 has been classified as Green List (High Evidence).","entity_name":"SPATA5","entity_type":"gene"},{"created":"2025-03-24T17:10:16.911153+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1756","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SPATA5 were changed from Epilepsy, hearing loss, and mental retardation syndrome, 616577 (3), Autosomal recessive to Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities, MIM# 616577","entity_name":"SPATA5","entity_type":"gene"},{"created":"2025-03-24T17:10:05.709752+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1755","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SPATA5 were set to ","entity_name":"SPATA5","entity_type":"gene"},{"created":"2025-03-24T17:09:33.134140+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1754","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMARCAL1 as ready","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2025-03-24T17:09:33.128327+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1754","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarcal1 has been classified as Green List (High Evidence).","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2025-03-24T17:09:30.164885+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1754","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMARCAL1 were changed from Schimke immunoosseous dysplasia, 242900 (3) to Schimke immunoosseous dysplasia, MIM# 242900","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2025-03-24T17:09:19.090245+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1753","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMARCAL1 were set to ","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2025-03-24T17:08:54.635180+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1752","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC6A8 as ready","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2025-03-24T17:08:54.629067+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1752","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc6a8 has been classified as Green List (High Evidence).","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2025-03-24T17:08:51.731832+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1752","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC6A8 were changed from Cerebral creatine deficiency syndrome 1, 300352 (3) to Cerebral creatine deficiency syndrome 1, MIM#300352","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2025-03-24T17:08:40.480006+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1751","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC6A8 were set to ","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2025-03-24T17:08:14.973541+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1750","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC6A5 as ready","entity_name":"SLC6A5","entity_type":"gene"},{"created":"2025-03-24T17:08:14.967606+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1750","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc6a5 has been classified as Green List (High Evidence).","entity_name":"SLC6A5","entity_type":"gene"},{"created":"2025-03-24T17:08:12.337766+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1750","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC6A5 were changed from Hyperekplexia 3, 614618 (3) to Hyperekplexia 3 MIM#614618","entity_name":"SLC6A5","entity_type":"gene"},{"created":"2025-03-24T17:07:55.344775+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1749","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC6A5 were set to ","entity_name":"SLC6A5","entity_type":"gene"},{"created":"2025-03-24T17:07:27.713640+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1748","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC52A3 as ready","entity_name":"SLC52A3","entity_type":"gene"},{"created":"2025-03-24T17:07:27.707002+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1748","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc52a3 has been classified as Green List (High Evidence).","entity_name":"SLC52A3","entity_type":"gene"},{"created":"2025-03-24T17:07:20.676628+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1748","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC52A3 were changed from Brown-Vialetto-Van Laere syndrome 1, 211530 (3) to Brown-Vialetto-Van Laere syndrome 1, MIM#211530","entity_name":"SLC52A3","entity_type":"gene"},{"created":"2025-03-24T17:07:09.916128+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1747","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC52A3 were set to ","entity_name":"SLC52A3","entity_type":"gene"},{"created":"2025-03-24T17:06:44.089408+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1746","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC52A2 as ready","entity_name":"SLC52A2","entity_type":"gene"},{"created":"2025-03-24T17:06:44.082116+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1746","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc52a2 has been classified as Green List (High Evidence).","entity_name":"SLC52A2","entity_type":"gene"},{"created":"2025-03-24T17:06:35.445110+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1746","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC52A2 were changed from Brown-Vialetto-Van Laere syndrome 2, 614707 (3) to Brown-Vialetto-Van Laere syndrome 2, MIM# 614707","entity_name":"SLC52A2","entity_type":"gene"},{"created":"2025-03-24T17:06:24.667697+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1745","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC52A2 were set to ","entity_name":"SLC52A2","entity_type":"gene"},{"created":"2025-03-24T17:05:57.535610+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1744","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC4A4 as ready","entity_name":"SLC4A4","entity_type":"gene"},{"created":"2025-03-24T17:05:57.524373+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1744","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc4a4 has been classified as Green List (High Evidence).","entity_name":"SLC4A4","entity_type":"gene"},{"created":"2025-03-24T17:05:54.426400+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1744","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC4A4 were changed from Renal tubular acidosis, proximal, with ocular abnormalities, 604278 (3) to Renal tubular acidosis, proximal, with ocular abnormalities, MIM#604278","entity_name":"SLC4A4","entity_type":"gene"},{"created":"2025-03-24T17:05:42.292758+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1743","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC4A4 were set to ","entity_name":"SLC4A4","entity_type":"gene"},{"created":"2025-03-24T17:05:12.659133+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1742","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC4A1 were changed from Distal renal tubular acidosis 4 with hemolytic anemia, MIM# 611590 to Distal renal tubular acidosis 4 with haemolytic anaemia, MIM# 611590","entity_name":"SLC4A1","entity_type":"gene"},{"created":"2025-03-24T17:04:09.142305+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1741","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC4A1 as ready","entity_name":"SLC4A1","entity_type":"gene"},{"created":"2025-03-24T17:04:09.135885+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1741","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc4a1 has been classified as Green List (High Evidence).","entity_name":"SLC4A1","entity_type":"gene"},{"created":"2025-03-24T17:04:06.147875+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1741","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC4A1 were changed from Renal tubular acidosis, distal, AR, 611590 (3) to Distal renal tubular acidosis 4 with hemolytic anemia, MIM# 611590","entity_name":"SLC4A1","entity_type":"gene"},{"created":"2025-03-24T17:03:41.791496+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1740","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC4A1 were set to ","entity_name":"SLC4A1","entity_type":"gene"},{"created":"2025-03-24T17:03:02.211962+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1739","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC33A1 as ready","entity_name":"SLC33A1","entity_type":"gene"},{"created":"2025-03-24T17:03:02.204886+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1739","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc33a1 has been classified as Green List (High Evidence).","entity_name":"SLC33A1","entity_type":"gene"},{"created":"2025-03-24T17:02:56.033628+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1739","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC33A1 were changed from Congenital cataracts, hearing loss, and neurodegeneration, 614482 (3) to Congenital cataracts, hearing loss, and neurodegeneration, MIM#614482","entity_name":"SLC33A1","entity_type":"gene"},{"created":"2025-03-24T17:02:45.814776+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1738","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC33A1 were set to ","entity_name":"SLC33A1","entity_type":"gene"},{"created":"2025-03-24T17:02:18.191893+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1737","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC26A3 as ready","entity_name":"SLC26A3","entity_type":"gene"},{"created":"2025-03-24T17:02:18.185247+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1737","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc26a3 has been classified as Green List (High Evidence).","entity_name":"SLC26A3","entity_type":"gene"},{"created":"2025-03-24T17:02:15.261904+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1737","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC26A3 were changed from Diarrhea 1, secretory chloride, congenital, 214700 (3) to Diarrhoea 1, secretory chloride, congenital MIM#214700","entity_name":"SLC26A3","entity_type":"gene"},{"created":"2025-03-24T17:02:00.263331+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1736","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC26A3 were set to ","entity_name":"SLC26A3","entity_type":"gene"},{"created":"2025-03-24T17:01:16.549338+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1735","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC25A13 as ready","entity_name":"SLC25A13","entity_type":"gene"},{"created":"2025-03-24T17:01:16.541892+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1735","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc25a13 has been classified as Green List (High Evidence).","entity_name":"SLC25A13","entity_type":"gene"},{"created":"2025-03-24T17:01:02.454956+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1735","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC25A13 were set to ","entity_name":"SLC25A13","entity_type":"gene"},{"created":"2025-03-24T16:59:01.843750+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.574","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KLC4 as ready","entity_name":"KLC4","entity_type":"gene"},{"created":"2025-03-24T16:59:01.836265+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.574","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: klc4 has been classified as Red List (Low Evidence).","entity_name":"KLC4","entity_type":"gene"},{"created":"2025-03-24T16:58:50.329956+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1734","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SKIV2L as ready","entity_name":"SKIV2L","entity_type":"gene"}]}