{"count":220790,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=994","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=992","results":[{"created":"2022-02-15T12:41:00.367986+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3459","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DBT were changed from MAPLE SYRUP URINE DISEASEQ to Maple syrup urine disease, type II (MIM#248600)","entity_name":"DBT","entity_type":"gene"},{"created":"2022-02-15T12:40:48.667561+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3458","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DBT were set to ","entity_name":"DBT","entity_type":"gene"},{"created":"2022-02-15T12:40:17.225987+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3457","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DARS2 as ready","entity_name":"DARS2","entity_type":"gene"},{"created":"2022-02-15T12:40:17.216701+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3457","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dars2 has been classified as Red List (Low Evidence).","entity_name":"DARS2","entity_type":"gene"},{"created":"2022-02-15T12:40:11.772639+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3457","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DARS2 were changed from LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION to Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation, MIM# 611105","entity_name":"DARS2","entity_type":"gene"},{"created":"2022-02-15T12:39:58.517913+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3456","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DARS2 were set to ","entity_name":"DARS2","entity_type":"gene"},{"created":"2022-02-15T12:39:19.282910+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3455","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC19 as ready","entity_name":"TTC19","entity_type":"gene"},{"created":"2022-02-15T12:39:19.267532+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3455","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc19 has been classified as Red List (Low Evidence).","entity_name":"TTC19","entity_type":"gene"},{"created":"2022-02-15T12:39:13.817983+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3455","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC19 were changed from MITOCHONDRIAL COMPLEX III DEFICIENCY to Mitochondrial complex III deficiency, nuclear type 2 (MIM#615157)","entity_name":"TTC19","entity_type":"gene"},{"created":"2022-02-15T12:39:01.929546+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3454","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC19 were set to ","entity_name":"TTC19","entity_type":"gene"},{"created":"2022-02-15T12:38:08.391573+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3453","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYP19A1 as ready","entity_name":"CYP19A1","entity_type":"gene"},{"created":"2022-02-15T12:38:08.380197+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3453","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyp19a1 has been classified as Red List (Low Evidence).","entity_name":"CYP19A1","entity_type":"gene"},{"created":"2022-02-15T12:38:04.110705+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3453","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CYP19A1 were changed from Aromatase deficiency 613546; Aromatase excess syndrome 139300 to Aromatase deficiency (MIM#613546), AR; Aromatase excess syndrome (MIM#139300), AD","entity_name":"CYP19A1","entity_type":"gene"},{"created":"2022-02-15T12:37:50.507228+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3452","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CYP19A1 were set to ","entity_name":"CYP19A1","entity_type":"gene"},{"created":"2022-02-15T12:37:39.479379+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3451","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CYP19A1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CYP19A1","entity_type":"gene"},{"created":"2022-02-15T12:37:05.023790+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3450","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TNXB as ready","entity_name":"TNXB","entity_type":"gene"},{"created":"2022-02-15T12:37:04.997533+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3450","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnxb has been classified as Red List (Low Evidence).","entity_name":"TNXB","entity_type":"gene"},{"created":"2022-02-15T12:36:44.280535+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3450","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TNXB were set to ","entity_name":"TNXB","entity_type":"gene"},{"created":"2022-02-15T12:36:27.228798+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3449","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TNXB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Vesicoureteral reflux 8, MIM#615963; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TNXB","entity_type":"gene"},{"created":"2022-02-15T12:33:52.863808+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10972","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FTSJ1 as ready","entity_name":"FTSJ1","entity_type":"gene"},{"created":"2022-02-15T12:33:52.851673+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10972","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ftsj1 has been classified as Green List (High Evidence).","entity_name":"FTSJ1","entity_type":"gene"},{"created":"2022-02-15T12:33:45.415423+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10972","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FTSJ1 were changed from  to Intellectual developmental disorder, X-linked 9 MIM#309549","entity_name":"FTSJ1","entity_type":"gene"},{"created":"2022-02-15T12:33:25.405990+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10971","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FTSJ1 were set to ","entity_name":"FTSJ1","entity_type":"gene"},{"created":"2022-02-15T12:32:28.987660+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10970","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FTSJ1 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"FTSJ1","entity_type":"gene"},{"created":"2022-02-15T12:31:51.985141+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3449","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLRT3 as ready","entity_name":"FLRT3","entity_type":"gene"},{"created":"2022-02-15T12:31:51.972875+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3449","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flrt3 has been classified as Red List (Low Evidence).","entity_name":"FLRT3","entity_type":"gene"},{"created":"2022-02-15T12:31:47.606202+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3449","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLRT3 were changed from Hypogonadotropic hypogonadism 21 with anosmia 615271 to Hypogonadotropic hypogonadism 21 with anosmia (MIM# 615271)","entity_name":"FLRT3","entity_type":"gene"},{"created":"2022-02-15T12:31:34.928988+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3448","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLRT3 were set to ","entity_name":"FLRT3","entity_type":"gene"},{"created":"2022-02-15T12:31:23.845914+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3447","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FLRT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FLRT3","entity_type":"gene"},{"created":"2022-02-15T12:30:51.457347+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3446","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM126B as ready","entity_name":"TMEM126B","entity_type":"gene"},{"created":"2022-02-15T12:30:51.443843+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3446","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem126b has been classified as Amber List (Moderate Evidence).","entity_name":"TMEM126B","entity_type":"gene"},{"created":"2022-02-15T12:30:47.659903+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3446","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM126B were changed from Muscle Weakness and Isolated Complex I Deficiency to Mitochondrial complex I deficiency, nuclear type 29 (MIM#618250)","entity_name":"TMEM126B","entity_type":"gene"},{"created":"2022-02-15T12:30:35.265118+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3445","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM126B were set to ","entity_name":"TMEM126B","entity_type":"gene"},{"created":"2022-02-15T12:30:23.596520+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3444","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TMEM126B as Amber List (moderate evidence)","entity_name":"TMEM126B","entity_type":"gene"},{"created":"2022-02-15T12:30:23.582031+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3444","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem126b has been classified as Amber List (Moderate Evidence).","entity_name":"TMEM126B","entity_type":"gene"},{"created":"2022-02-15T12:28:55.387531+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10969","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLAD1 as ready","entity_name":"FLAD1","entity_type":"gene"},{"created":"2022-02-15T12:28:55.374816+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10969","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flad1 has been classified as Green List (High Evidence).","entity_name":"FLAD1","entity_type":"gene"},{"created":"2022-02-15T12:28:47.552292+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10969","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLAD1 were changed from  to Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency MIM#255100","entity_name":"FLAD1","entity_type":"gene"},{"created":"2022-02-15T12:28:27.609051+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10968","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLAD1 were set to ","entity_name":"FLAD1","entity_type":"gene"},{"created":"2022-02-15T12:28:08.282285+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10967","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FLAD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FLAD1","entity_type":"gene"},{"created":"2022-02-15T12:27:34.342211+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3443","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLAD1 as ready","entity_name":"FLAD1","entity_type":"gene"},{"created":"2022-02-15T12:27:34.332191+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3443","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flad1 has been classified as Red List (Low Evidence).","entity_name":"FLAD1","entity_type":"gene"},{"created":"2022-02-15T12:27:30.809744+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3443","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLAD1 were changed from Riboflavin-Responsive and Non-responsive Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency. to Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency MIM#255100","entity_name":"FLAD1","entity_type":"gene"},{"created":"2022-02-15T12:27:15.214996+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3442","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLAD1 were set to ","entity_name":"FLAD1","entity_type":"gene"},{"created":"2022-02-15T12:26:45.231098+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3441","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TK2 as ready","entity_name":"TK2","entity_type":"gene"},{"created":"2022-02-15T12:26:45.216199+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3441","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tk2 has been classified as Red List (Low Evidence).","entity_name":"TK2","entity_type":"gene"},{"created":"2022-02-15T12:26:41.098811+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3441","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TK2 were changed from MITOCHONDRIAL DNA DEPLETION SYNDROME, MYOPATHIC FORM to Mitochondrial DNA depletion syndrome 2 (myopathic type) (MIM#609560)","entity_name":"TK2","entity_type":"gene"},{"created":"2022-02-15T12:26:01.363721+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3440","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGF20 as ready","entity_name":"FGF20","entity_type":"gene"},{"created":"2022-02-15T12:26:01.353450+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3440","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgf20 has been classified as Amber List (Moderate Evidence).","entity_name":"FGF20","entity_type":"gene"},{"created":"2022-02-15T12:25:57.562766+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3440","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGF20 were changed from ?Renal hypodysplasia/aplasia 2, 615721 to Renal hypodysplasia/aplasia 2, MIM#615721","entity_name":"FGF20","entity_type":"gene"},{"created":"2022-02-15T12:25:25.474591+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3439","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FGF20 as Amber List (moderate evidence)","entity_name":"FGF20","entity_type":"gene"},{"created":"2022-02-15T12:25:25.455570+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3439","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgf20 has been classified as Amber List (Moderate Evidence).","entity_name":"FGF20","entity_type":"gene"},{"created":"2022-02-15T12:24:40.120927+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3438","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGF17 as ready","entity_name":"FGF17","entity_type":"gene"},{"created":"2022-02-15T12:24:40.109309+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3438","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgf17 has been classified as Red List (Low Evidence).","entity_name":"FGF17","entity_type":"gene"},{"created":"2022-02-15T12:24:34.313571+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3438","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FGF17 were set to ","entity_name":"FGF17","entity_type":"gene"},{"created":"2022-02-15T12:24:22.118504+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3437","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGF17 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGF17","entity_type":"gene"},{"created":"2022-02-15T12:23:52.061239+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3436","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TEK as ready","entity_name":"TEK","entity_type":"gene"},{"created":"2022-02-15T12:23:52.050745+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3436","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tek has been classified as Red List (Low Evidence).","entity_name":"TEK","entity_type":"gene"},{"created":"2022-02-15T12:23:48.494407+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3436","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TEK were changed from VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL to Glaucoma 3, primary congenital, E (MIM#617272); Venous malformations, multiple cutaneous and mucosal (MIM#600195)","entity_name":"TEK","entity_type":"gene"},{"created":"2022-02-15T12:23:35.297477+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3435","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TEK were set to ","entity_name":"TEK","entity_type":"gene"},{"created":"2022-02-15T12:22:37.626095+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10966","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGF17 as ready","entity_name":"FGF17","entity_type":"gene"},{"created":"2022-02-15T12:22:37.614678+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10966","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgf17 has been classified as Green List (High Evidence).","entity_name":"FGF17","entity_type":"gene"},{"created":"2022-02-15T12:22:19.955114+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10966","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGF17 were changed from  to Hypogonadotropic hypogonadism 20 with or without anosmia MIM#615270","entity_name":"FGF17","entity_type":"gene"},{"created":"2022-02-15T12:21:57.225396+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10965","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FGF17 were set to ","entity_name":"FGF17","entity_type":"gene"},{"created":"2022-02-15T12:21:10.607069+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10964","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGF17 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGF17","entity_type":"gene"},{"created":"2022-02-15T12:12:20.442658+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3434","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBXAS1 were changed from Ghosal hematodiaphyseal syndrome (MIM#231095) to Ghosal haematodiaphyseal syndrome (MIM#231095)","entity_name":"TBXAS1","entity_type":"gene"},{"created":"2022-02-15T12:12:07.831659+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3433","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBXAS1 as ready","entity_name":"TBXAS1","entity_type":"gene"},{"created":"2022-02-15T12:12:07.819596+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3433","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbxas1 has been classified as Red List (Low Evidence).","entity_name":"TBXAS1","entity_type":"gene"},{"created":"2022-02-15T12:12:04.226770+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3433","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBXAS1 were changed from GHOSAL HEMATODIAPHYSEAL SYNDROME to Ghosal hematodiaphyseal syndrome (MIM#231095)","entity_name":"TBXAS1","entity_type":"gene"},{"created":"2022-02-15T12:11:25.711356+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3432","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TANGO2 as ready","entity_name":"TANGO2","entity_type":"gene"},{"created":"2022-02-15T12:11:25.700020+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3432","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tango2 has been classified as Red List (Low Evidence).","entity_name":"TANGO2","entity_type":"gene"},{"created":"2022-02-15T12:11:21.628732+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3432","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TANGO2 were changed from Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy to Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration (MIM#616878)","entity_name":"TANGO2","entity_type":"gene"},{"created":"2022-02-15T12:11:06.053455+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3431","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TANGO2 were set to ","entity_name":"TANGO2","entity_type":"gene"},{"created":"2022-02-15T12:10:49.506813+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3430","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TANGO2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration (MIM#616878); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TANGO2","entity_type":"gene"},{"created":"2022-02-15T12:10:06.144795+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3430","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZFYVE26 as ready","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2022-02-15T12:10:06.130882+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3430","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zfyve26 has been classified as Red List (Low Evidence).","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2022-02-15T12:10:01.852802+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3430","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZFYVE26 were changed from SPASTIC PARAPLEGIA AUTOSOMAL RECESSIVE TYPE 15 to Spastic paraplegia 15, autosomal recessive MIM#270700","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2022-02-15T12:09:47.227318+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3429","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZFYVE26 were set to ","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2022-02-15T12:09:28.596111+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3428","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZFYVE26: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Spastic paraplegia 15, autosomal recessive MIM#270700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2022-02-15T11:50:18.109844+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SYP as ready","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:50:18.098436+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: syp has been classified as Green List (High Evidence).","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:50:02.946964+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4503","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SYP were changed from  to Mental retardation, X-linked 96 MIM#300802","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:49:28.472018+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4502","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SYP were set to ","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:48:54.570295+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4501","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SYP was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:48:21.879772+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4500","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SYP: Rating: GREEN; Mode of pathogenicity: None; Publications: 23966691, 19377476; Phenotypes: Mental retardation, X-linked 96 MIM#300802; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:46:53.166951+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10963","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SYP as ready","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:46:53.157655+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10963","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: syp has been classified as Green List (High Evidence).","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:46:45.656303+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10963","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SYP were changed from  to Mental retardation, X-linked 96 MIM#300802","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:46:24.984121+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10962","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SYP were set to ","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:46:05.307457+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10961","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: SYP was changed from  to None","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:45:47.134746+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10960","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SYP was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:44:48.706769+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3428","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SYP as ready","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:44:48.683270+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3428","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: syp has been classified as Red List (Low Evidence).","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:44:45.216258+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3428","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SYP were changed from MENTAL RETARDATION X-LINKED SYP-RELATED to Intellectual developmental disorder, X-linked 96 (MIM#300802)","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:44:32.875920+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3427","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SYP were set to ","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:44:17.855480+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3426","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SYP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SYP","entity_type":"gene"},{"created":"2022-02-15T11:43:34.759749+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3426","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYC1 as ready","entity_name":"CYC1","entity_type":"gene"},{"created":"2022-02-15T11:43:34.750302+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3426","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyc1 has been classified as Red List (Low Evidence).","entity_name":"CYC1","entity_type":"gene"},{"created":"2022-02-15T11:43:31.248042+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3426","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CYC1 were changed from MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 to Mitochondrial complex III deficiency, nuclear type 6, MIM# 615453","entity_name":"CYC1","entity_type":"gene"},{"created":"2022-02-15T11:43:19.018244+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3425","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CYC1 were set to ","entity_name":"CYC1","entity_type":"gene"}]}