{"count":220423,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=793","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=791","results":[{"created":"2022-07-21T12:49:47.779439+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.58","user_name":"Crystle Lee","item_type":"entity","text":"reviewed gene: C6: Rating: AMBER; Mode of pathogenicity: None; Publications: 31440263, 23537992, 17257682, 22668955, 32670577; Phenotypes: C6 deficiency (MIM#612446); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"C6","entity_type":"gene"},{"created":"2022-07-21T12:38:43.812691+10:00","panel_name":"Complement Deficiencies","panel_id":224,"panel_version":"0.72","user_name":"Crystle Lee","item_type":"entity","text":"reviewed gene: C5: Rating: AMBER; Mode of pathogenicity: None; Publications: 31440263, 23743184, 15488949, 15778377, 23371790; Phenotypes: C5 deficiency (MIM#609536); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"C5","entity_type":"gene"},{"created":"2022-07-21T11:45:57.607601+10:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.114","user_name":"Peter McNaughton","item_type":"entity","text":"reviewed gene: IL23R: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 35829840; Phenotypes: Susceptibility to mycobacterial disease; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IL23R","entity_type":"gene"},{"created":"2022-07-21T11:37:40.442832+10:00","panel_name":"Phagocyte Defects","panel_id":233,"panel_version":"1.4","user_name":"Peter McNaughton","item_type":"entity","text":"reviewed gene: HYOU1: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 35822684; Phenotypes: Severe congenital neutropaenia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HYOU1","entity_type":"gene"},{"created":"2022-07-21T11:32:14.817019+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.58","user_name":"Crystle Lee","item_type":"entity","text":"reviewed gene: PGK1: Rating: ; Mode of pathogenicity: None; Publications: 16567715, 30887539, 22348148, 28580215; Phenotypes: Phosphoglycerate kinase 1 deficiency (MIM#300653); Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"PGK1","entity_type":"gene"},{"created":"2022-07-21T11:02:35.303270+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.58","user_name":"Crystle Lee","item_type":"entity","text":"reviewed gene: GK: Rating: AMBER; Mode of pathogenicity: None; Publications: 33212314, 16549535, 10851254, 9719371, 8651297; Phenotypes: Glycerol kinase deficiency (MIM#307030); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GK","entity_type":"gene"},{"created":"2022-07-20T20:16:13.865365+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.284","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UROS were set to 24027798","entity_name":"UROS","entity_type":"gene"},{"created":"2022-07-20T20:15:36.024783+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.283","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UROS as Green List (high evidence)","entity_name":"UROS","entity_type":"gene"},{"created":"2022-07-20T20:15:36.016361+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.283","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uros has been classified as Green List (High Evidence).","entity_name":"UROS","entity_type":"gene"},{"created":"2022-07-20T17:03:29.140536+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.282","user_name":"Chern Lim","item_type":"entity","text":"reviewed gene: UROS: Rating: GREEN; Mode of pathogenicity: None; Publications: 30685241, 34828434, 15065102, 11254675; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"UROS","entity_type":"gene"},{"created":"2022-07-20T16:59:09.356918+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: HERC2.","entity_name":"HERC2","entity_type":"gene"},{"created":"2022-07-20T16:57:43.938518+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: GBA.","entity_name":"GBA","entity_type":"gene"},{"created":"2022-07-20T16:54:52.406148+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SAMD9 as ready","entity_name":"SAMD9","entity_type":"gene"},{"created":"2022-07-20T16:54:52.395694+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: samd9 has been classified as Red List (Low Evidence).","entity_name":"SAMD9","entity_type":"gene"},{"created":"2022-07-20T16:54:09.497806+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SAMD9 were set to ","entity_name":"SAMD9","entity_type":"gene"},{"created":"2022-07-20T16:53:57.662216+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SAMD9 as Red List (low evidence)","entity_name":"SAMD9","entity_type":"gene"},{"created":"2022-07-20T16:53:57.648834+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: samd9 has been classified as Red List (Low Evidence).","entity_name":"SAMD9","entity_type":"gene"},{"created":"2022-07-20T16:53:11.312488+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: FTCD.","entity_name":"FTCD","entity_type":"gene"},{"created":"2022-07-20T16:51:19.705068+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT85 as ready","entity_name":"KRT85","entity_type":"gene"},{"created":"2022-07-20T16:51:19.695277+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt85 has been classified as Red List (Low Evidence).","entity_name":"KRT85","entity_type":"gene"},{"created":"2022-07-20T16:51:05.082060+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KRT85 as Red List (low evidence)","entity_name":"KRT85","entity_type":"gene"},{"created":"2022-07-20T16:51:05.064734+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt85 has been classified as Red List (Low Evidence).","entity_name":"KRT85","entity_type":"gene"},{"created":"2022-07-20T16:50:45.879176+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT85: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ectodermal dysplasia 4, hair/nail type (MIM#602032); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KRT85","entity_type":"gene"},{"created":"2022-07-20T16:40:10.930193+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAG2 as ready","entity_name":"RAG2","entity_type":"gene"},{"created":"2022-07-20T16:40:10.914296+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rag2 has been classified as Green List (High Evidence).","entity_name":"RAG2","entity_type":"gene"},{"created":"2022-07-20T16:40:05.311708+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAG2 were set to ","entity_name":"RAG2","entity_type":"gene"},{"created":"2022-07-20T16:38:38.128944+10:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PPP1R13L were changed from Dilated cardiomyopathy, onset in infancy to Multiple congenital anomalies/dysmorphic syndrome, MONDO:0019042 - PPP1R13L-related; Dilated cardiomyopathy, onset in infancy","entity_name":"PPP1R13L","entity_type":"gene"},{"created":"2022-07-20T16:38:08.830411+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.164","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PPP1R13L were changed from Dilated cardiomyopathy, onset in infancy to Multiple congenital anomalies/dysmorphic syndrome, MONDO:0019042 - PPP1R13L-related; Dilated cardiomyopathy, onset in infancy","entity_name":"PPP1R13L","entity_type":"gene"},{"created":"2022-07-20T16:37:41.598976+10:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.183","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PPP1R13L were changed from Dilated cardiomyopathy, onset in infancy; Cleft lip and palate to Multiple congenital anomalies/dysmorphic syndrome, MONDO:0019042 - PPP1R13L-related; Dilated cardiomyopathy, onset in infancy; Cleft lip and palate","entity_name":"PPP1R13L","entity_type":"gene"},{"created":"2022-07-20T16:37:18.494702+10:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.48","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PPP1R13L were changed from Dilated cardiomyopathy, onset in infancy; Cleft lip and palate to Multiple congenital anomalies/dysmorphic syndrome, MONDO:0019042 - PPP1R13L-related; Dilated cardiomyopathy, onset in infancy; Cleft lip and palate","entity_name":"PPP1R13L","entity_type":"gene"},{"created":"2022-07-20T16:36:35.257653+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: CARD9.","entity_name":"CARD9","entity_type":"gene"},{"created":"2022-07-20T16:34:15.709717+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: PLG.","entity_name":"PLG","entity_type":"gene"},{"created":"2022-07-20T16:32:49.878745+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: GYS2.","entity_name":"GYS2","entity_type":"gene"},{"created":"2022-07-20T16:30:56.161921+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: MPZ.","entity_name":"MPZ","entity_type":"gene"},{"created":"2022-07-20T16:27:53.271183+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.215","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: KIAA1161.","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2022-07-20T14:05:51.362974+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Crystle Lee","item_type":"entity","text":"reviewed gene: HERC2: Rating: AMBER; Mode of pathogenicity: None; Publications: 31124564, 11896453; Phenotypes: Intellectual developmental disorder, autosomal recessive 38 (MIM#615516); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HERC2","entity_type":"gene"},{"created":"2022-07-20T13:38:23.644132+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Crystle Lee","item_type":"entity","text":"reviewed gene: GBA: Rating: AMBER; Mode of pathogenicity: None; Publications: 28727984; Phenotypes: Gaucher disease, perinatal lethal (MIM#608013); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GBA","entity_type":"gene"},{"created":"2022-07-20T13:28:43.554622+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.215","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIAA1161 as ready","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2022-07-20T13:28:43.543571+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.215","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiaa1161 has been classified as Green List (High Evidence).","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2022-07-20T13:28:11.331040+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.215","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIAA1161 were changed from Primary familial brain calcification; Atypical parkinsonism; Supranuclear gaze palsy; OMIM 618317 to Basal ganglia calcification, idiopathic, 7, autosomal recessive, OMIM #618317; Primary familial brain calcification; Atypical parkinsonism; Supranuclear gaze palsy","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2022-07-20T13:27:23.028606+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.214","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIAA1161 were set to PMID: 32211515","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2022-07-20T13:26:28.380583+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.213","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIAA1161 as Green List (high evidence)","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2022-07-20T13:26:28.368358+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.213","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiaa1161 has been classified as Green List (High Evidence).","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2022-07-20T13:25:52.750983+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.212","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KIAA1161: Rating: GREEN; Mode of pathogenicity: None; Publications: 30656188, 30649222, 30460687, 29910000, 31951047; Phenotypes: Basal ganglia calcification, idiopathic, 7, autosomal recessive, OMIM #618317; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KIAA1161","entity_type":"gene"},{"created":"2022-07-20T13:23:27.107992+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.212","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NHLRC1 as ready","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2022-07-20T13:23:27.092637+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.212","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nhlrc1 has been classified as Amber List (Moderate Evidence).","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2022-07-20T13:23:24.409506+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.212","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NHLRC1 were changed from Lafora disease; Progressive Myoclonic Epilepsy; Parkinsonism; OMIM 254780 to Epilepsy, progressive myoclonic 2B (Lafora), MIM# 254780; Lafora disease; Progressive Myoclonic Epilepsy; Parkinsonism","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2022-07-20T13:22:36.353988+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NHLRC1 as Amber List (moderate evidence)","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2022-07-20T13:22:36.341901+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nhlrc1 has been classified as Amber List (Moderate Evidence).","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2022-07-20T13:22:03.476227+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.210","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NHLRC1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Epilepsy, progressive myoclonic 2B (Lafora), MIM# 254780; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2022-07-20T13:19:05.523286+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.210","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: C9orf3.","entity_name":"C9orf3","entity_type":"gene"},{"created":"2022-07-20T13:18:37.761691+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.210","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C9orf3 as ready","entity_name":"C9orf3","entity_type":"gene"},{"created":"2022-07-20T13:18:37.752554+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.210","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c9orf3 has been classified as Green List (High Evidence).","entity_name":"C9orf3","entity_type":"gene"},{"created":"2022-07-20T13:18:30.728203+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.210","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C9orf3 were changed from Dystonia-31; Childhood/Adolescence onset generalised dystonia; Dystonia parkinsonism; Zech-Boesch Syndrome; OMIM 619565 to Dystonia 31, MIM# 619565; Childhood/Adolescence onset generalised dystonia; Dystonia parkinsonism; Zech-Boesch Syndrome","entity_name":"C9orf3","entity_type":"gene"},{"created":"2022-07-20T13:17:40.153527+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.209","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: C9orf3 as Green List (high evidence)","entity_name":"C9orf3","entity_type":"gene"},{"created":"2022-07-20T13:17:40.142368+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.209","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c9orf3 has been classified as Green List (High Evidence).","entity_name":"C9orf3","entity_type":"gene"},{"created":"2022-07-20T13:17:07.047635+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: C9orf3: Rating: GREEN; Mode of pathogenicity: None; Publications: 35306330; Phenotypes: Dystonia 31, MIM# 619565; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"C9orf3","entity_type":"gene"},{"created":"2022-07-20T13:13:05.253436+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: NCF1.","entity_name":"NCF1","entity_type":"gene"},{"created":"2022-07-20T13:12:31.290002+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: NEB.","entity_name":"NEB","entity_type":"gene"},{"created":"2022-07-20T13:11:58.043599+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: HYDIN.","entity_name":"HYDIN","entity_type":"gene"},{"created":"2022-07-20T13:10:33.919518+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SNORD118 as ready","entity_name":"SNORD118","entity_type":"gene"},{"created":"2022-07-20T13:10:33.907833+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snord118 has been classified as Red List (Low Evidence).","entity_name":"SNORD118","entity_type":"gene"},{"created":"2022-07-20T13:10:23.907011+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SNORD118 were set to ","entity_name":"SNORD118","entity_type":"gene"},{"created":"2022-07-20T13:10:07.891157+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SNORD118 as Red List (low evidence)","entity_name":"SNORD118","entity_type":"gene"},{"created":"2022-07-20T13:10:07.882096+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snord118 has been classified as Red List (Low Evidence).","entity_name":"SNORD118","entity_type":"gene"},{"created":"2022-07-20T13:09:54.336477+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SNORD118: Rating: RED; Mode of pathogenicity: None; Publications: 32361877, 33029936; Phenotypes: Leukoencephalopathy, brain calcifications, and cysts, MIM#614561; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SNORD118","entity_type":"gene"},{"created":"2022-07-20T13:07:29.719424+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBA1 as ready","entity_name":"UBA1","entity_type":"gene"},{"created":"2022-07-20T13:07:29.710035+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uba1 has been classified as Green List (High Evidence).","entity_name":"UBA1","entity_type":"gene"},{"created":"2022-07-20T13:05:51.392834+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBA1 were set to ","entity_name":"UBA1","entity_type":"gene"},{"created":"2022-07-20T13:03:12.408342+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: CHM.","entity_name":"CHM","entity_type":"gene"},{"created":"2022-07-20T13:01:39.974721+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: PROC.","entity_name":"PROC","entity_type":"gene"},{"created":"2022-07-20T13:00:20.525240+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IKBKG as ready","entity_name":"IKBKG","entity_type":"gene"},{"created":"2022-07-20T13:00:20.516753+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ikbkg has been classified as Amber List (Moderate Evidence).","entity_name":"IKBKG","entity_type":"gene"},{"created":"2022-07-20T12:59:59.661082+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IKBKG as Amber List (moderate evidence)","entity_name":"IKBKG","entity_type":"gene"},{"created":"2022-07-20T12:59:59.648621+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ikbkg has been classified as Amber List (Moderate Evidence).","entity_name":"IKBKG","entity_type":"gene"},{"created":"2022-07-20T12:59:44.299858+10:00","panel_name":"Reproductive Carrier Screen_VCGS","panel_id":3861,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IKBKG: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"IKBKG","entity_type":"gene"},{"created":"2022-07-20T12:58:23.087081+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATXN10 as ready","entity_name":"ATXN10","entity_type":"gene"},{"created":"2022-07-20T12:58:23.077708+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atxn10 has been removed from the panel.","entity_name":"ATXN10","entity_type":"gene"},{"created":"2022-07-20T12:58:18.359501+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"Tag STR tag was added to gene: ATXN10.","entity_name":"ATXN10","entity_type":"gene"},{"created":"2022-07-20T12:57:57.552499+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: ATXN10","entity_name":"ATXN10","entity_type":"gene"},{"created":"2022-07-20T12:57:15.048559+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATXN2 as ready","entity_name":"ATXN2","entity_type":"gene"},{"created":"2022-07-20T12:57:15.029374+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atxn2 has been removed from the panel.","entity_name":"ATXN2","entity_type":"gene"},{"created":"2022-07-20T12:57:04.571716+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ATXN2 were set to PMID: 11761482, 17923635","entity_name":"ATXN2","entity_type":"gene"},{"created":"2022-07-20T12:56:30.927675+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"Tag STR tag was added to gene: ATXN2.","entity_name":"ATXN2","entity_type":"gene"},{"created":"2022-07-20T12:56:16.823831+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: ATXN2","entity_name":"ATXN2","entity_type":"gene"},{"created":"2022-07-20T12:55:38.006561+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"Tag STR tag was added to gene: ATXN3.","entity_name":"ATXN3","entity_type":"gene"},{"created":"2022-07-20T12:55:31.703956+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATXN3 as ready","entity_name":"ATXN3","entity_type":"gene"},{"created":"2022-07-20T12:55:31.694978+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atxn3 has been removed from the panel.","entity_name":"ATXN3","entity_type":"gene"},{"created":"2022-07-20T12:55:22.153376+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: ATXN3","entity_name":"ATXN3","entity_type":"gene"},{"created":"2022-07-20T12:54:18.772449+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATXN8 as ready","entity_name":"ATXN8","entity_type":"gene"},{"created":"2022-07-20T12:54:18.761108+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atxn8 has been removed from the panel.","entity_name":"ATXN8","entity_type":"gene"},{"created":"2022-07-20T12:54:12.092619+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"Tag STR tag was added to gene: ATXN8.","entity_name":"ATXN8","entity_type":"gene"},{"created":"2022-07-20T12:54:02.194206+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: ATXN8","entity_name":"ATXN8","entity_type":"gene"},{"created":"2022-07-20T12:52:22.493699+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TPP1 as ready","entity_name":"TPP1","entity_type":"gene"},{"created":"2022-07-20T12:52:22.485238+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tpp1 has been classified as Green List (High Evidence).","entity_name":"TPP1","entity_type":"gene"},{"created":"2022-07-20T12:52:19.335176+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TPP1 were changed from Late Infantile NCL; Parkinsonism; OMIM 204500 to Ceroid lipofuscinosis, neuronal, 2, MIM# 204500; Parkinsonism","entity_name":"TPP1","entity_type":"gene"},{"created":"2022-07-20T12:51:38.081844+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.206","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TPP1 as Green List (high evidence)","entity_name":"TPP1","entity_type":"gene"},{"created":"2022-07-20T12:51:38.064511+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.206","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tpp1 has been classified as Green List (High Evidence).","entity_name":"TPP1","entity_type":"gene"},{"created":"2022-07-20T12:51:05.197983+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.205","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TPP1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Ceroid lipofuscinosis, neuronal, 2, MIM# 204500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TPP1","entity_type":"gene"},{"created":"2022-07-20T12:49:37.320608+10:00","panel_name":"Early-onset Parkinson disease","panel_id":26,"panel_version":"0.205","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYP27A1 as ready","entity_name":"CYP27A1","entity_type":"gene"}]}