{"count":220790,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1989","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1987","results":[{"created":"2020-01-14T14:15:35.742995+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MLH1 as ready","entity_name":"MLH1","entity_type":"gene"},{"created":"2020-01-14T14:15:35.729578+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mlh1 has been classified as Red List (Low Evidence).","entity_name":"MLH1","entity_type":"gene"},{"created":"2020-01-14T14:14:59.807598+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MNX1 as ready","entity_name":"MNX1","entity_type":"gene"},{"created":"2020-01-14T14:14:59.795903+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mnx1 has been classified as Red List (Low Evidence).","entity_name":"MNX1","entity_type":"gene"},{"created":"2020-01-14T14:14:29.250958+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MPZ as ready","entity_name":"MPZ","entity_type":"gene"},{"created":"2020-01-14T14:14:29.239601+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mpz has been classified as Red List (Low Evidence).","entity_name":"MPZ","entity_type":"gene"},{"created":"2020-01-14T14:13:51.693832+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MRAP as ready","entity_name":"MRAP","entity_type":"gene"},{"created":"2020-01-14T14:13:51.681510+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mrap has been classified as Red List (Low Evidence).","entity_name":"MRAP","entity_type":"gene"},{"created":"2020-01-14T13:51:12.130343+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: WHRN was added\ngene: WHRN was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: WHRN was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: WHRN were set to Usher syndrome, type 2D, 611383","entity_name":"WHRN","entity_type":"gene"},{"created":"2020-01-14T13:51:12.055274+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: USH2A was added\ngene: USH2A was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: USH2A was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: USH2A were set to Usher syndrome, type 2A, 276901; Retinitis pigmentosa 39, 613809","entity_name":"USH2A","entity_type":"gene"},{"created":"2020-01-14T13:51:11.972987+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: USH1G was added\ngene: USH1G was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: USH1G was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: USH1G were set to Usher syndrome, type 1G, 606943","entity_name":"USH1G","entity_type":"gene"},{"created":"2020-01-14T13:51:11.897608+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: USH1C was added\ngene: USH1C was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: USH1C was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: USH1C were set to Usher syndrome, type 1C, 276904","entity_name":"USH1C","entity_type":"gene"},{"created":"2020-01-14T13:51:11.823090+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PEX6 was added\ngene: PEX6 was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PEX6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PEX6 were set to Heimler syndrome 2, 616617","entity_name":"PEX6","entity_type":"gene"},{"created":"2020-01-14T13:51:11.748998+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PEX1 was added\ngene: PEX1 was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PEX1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PEX1 were set to Heimler syndrome 1, 234580","entity_name":"PEX1","entity_type":"gene"},{"created":"2020-01-14T13:51:11.676781+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PDZD7 was added\ngene: PDZD7 was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PDZD7 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PDZD7 were set to Usher syndrome, type IIC, GPR98/PDZD7 digenic, 605472","entity_name":"PDZD7","entity_type":"gene"},{"created":"2020-01-14T13:51:11.597246+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PCDH15 was added\ngene: PCDH15 was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PCDH15 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PCDH15 were set to Usher syndrome Type 1F; Usher syndrome, type 1D/F digenic","entity_name":"PCDH15","entity_type":"gene"},{"created":"2020-01-14T13:51:11.523788+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: MYO7A was added\ngene: MYO7A was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: MYO7A was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: MYO7A were set to Usher syndrome, type 1B, 276900","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-01-14T13:51:11.451037+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: HARS was added\ngene: HARS was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: HARS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HARS were set to Usher syndrome type 3B","entity_name":"HARS","entity_type":"gene"},{"created":"2020-01-14T13:51:11.378673+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ESPN was added\ngene: ESPN was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ESPN was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ESPN were set to ?Usher syndrome, type 1M, 618632; Deafness, autosomal recessive 36, 609006","entity_name":"ESPN","entity_type":"gene"},{"created":"2020-01-14T13:51:11.304900+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CLRN1 was added\ngene: CLRN1 was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CLRN1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CLRN1 were set to ?Usher syndrome, type 3A, 276902Retinitis pigmentosa 61, 614180","entity_name":"CLRN1","entity_type":"gene"},{"created":"2020-01-14T13:51:11.232997+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CIB2 was added\ngene: CIB2 was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CIB2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CIB2 were set to Usher syndrome, type IJ, 614869","entity_name":"CIB2","entity_type":"gene"},{"created":"2020-01-14T13:51:11.161812+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CEP78 was added\ngene: CEP78 was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CEP78 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CEP78 were set to Cone-Rod Dystrophy and Hearing Loss, 617236","entity_name":"CEP78","entity_type":"gene"},{"created":"2020-01-14T13:51:11.087970+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CEP250 was added\ngene: CEP250 was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CEP250 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CEP250 were set to Usher-like disease; Cone-rod dystrophy and hearing loss 2, 618358","entity_name":"CEP250","entity_type":"gene"},{"created":"2020-01-14T13:51:11.014509+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CDH23 was added\ngene: CDH23 was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CDH23 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CDH23 were set to Usher syndrome, type 1D 601067; Usher syndrome, type 1D/F digenic 601067","entity_name":"CDH23","entity_type":"gene"},{"created":"2020-01-14T13:51:10.940958+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ARSG was added\ngene: ARSG was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ARSG was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARSG were set to Usher syndrome, type IV, 618144","entity_name":"ARSG","entity_type":"gene"},{"created":"2020-01-14T13:51:10.868747+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ADGRV1 was added\ngene: ADGRV1 was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ADGRV1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ADGRV1 were set to Usher syndrome,  type 2C","entity_name":"ADGRV1","entity_type":"gene"},{"created":"2020-01-14T13:51:10.795601+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ABHD12 was added\ngene: ABHD12 was added to Usher Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ABHD12 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ABHD12 were set to Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract, 614857; Usher syndrome type 3","entity_name":"ABHD12","entity_type":"gene"},{"created":"2020-01-14T13:51:10.750287+11:00","panel_name":"Usher Syndrome_RMH","panel_id":3086,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"panel","text":"Added panel Usher Syndrome_RMH","entity_name":null,"entity_type":null},{"created":"2020-01-14T13:20:50.784157+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: TYMP was added\ngene: TYMP was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: TYMP was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TYMP were set to Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) 612073","entity_name":"TYMP","entity_type":"gene"},{"created":"2020-01-14T13:20:50.708664+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: TSFM was added\ngene: TSFM was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: TSFM was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TSFM were set to Combined oxidative phosphorylation deficiency 3 610505","entity_name":"TSFM","entity_type":"gene"},{"created":"2020-01-14T13:20:50.630507+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: TSEN54 was added\ngene: TSEN54 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: TSEN54 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TSEN54 were set to ?Pontocerebellar hypoplasia type 5 610204; Pontocerebellar hypoplasia type 4 225753; Pontocerebellar hypoplasia type 2A 277470","entity_name":"TSEN54","entity_type":"gene"},{"created":"2020-01-14T13:20:50.552532+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: TK2 was added\ngene: TK2 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: TK2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TK2 were set to Mitochondrial DNA depletion syndrome 2 (myopathic type), 609560","entity_name":"TK2","entity_type":"gene"},{"created":"2020-01-14T13:20:50.476270+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: TANGO2 was added\ngene: TANGO2 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: TANGO2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TANGO2 were set to Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration, 616878","entity_name":"TANGO2","entity_type":"gene"},{"created":"2020-01-14T13:20:50.401266+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SUCLA2 was added\ngene: SUCLA2 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: SUCLA2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: SUCLA2 were set to Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) 612073","entity_name":"SUCLA2","entity_type":"gene"},{"created":"2020-01-14T13:20:50.326505+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SLC22A5 was added\ngene: SLC22A5 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: SLC22A5 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: SLC22A5 were set to Carnitine deficiency, systemic primary 212140","entity_name":"SLC22A5","entity_type":"gene"},{"created":"2020-01-14T13:20:50.251739+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SIL1 was added\ngene: SIL1 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: SIL1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: SIL1 were set to Marinesco-Sjogren syndrome 248800","entity_name":"SIL1","entity_type":"gene"},{"created":"2020-01-14T13:20:50.174391+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SCN4A was added\ngene: SCN4A was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: SCN4A was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: SCN4A were set to Paramyotonia congenita, 168300; Myotonia congenita, atypical, acetazolamide-responsive, 608390; Hypokalemic periodic paralysis, type 2, 613345; Myasthenic syndrome, congenital, 16, 614198; Hyperkalemic periodic paralysis, type 2, 170500","entity_name":"SCN4A","entity_type":"gene"},{"created":"2020-01-14T13:20:50.099236+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RYR1 was added\ngene: RYR1 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RYR1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: RYR1 were set to {Malignant hyperthermia susceptibility 1}, 145600; Central core disease, 117000; King-Denborough syndrome, 145600; Neuromuscular disease, congenital, with uniform type 1 fiber, 117000; Minicore myopathy with external ophthalmoplegia, 255320","entity_name":"RYR1","entity_type":"gene"},{"created":"2020-01-14T13:20:50.017743+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RRM2B was added\ngene: RRM2B was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RRM2B was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: RRM2B were set to Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy), 612075; Mitochondrial DNA depletion syndrome 8B (MNGIE type), 612075; Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5, 613077","entity_name":"RRM2B","entity_type":"gene"},{"created":"2020-01-14T13:20:49.937414+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RBCK1 was added\ngene: RBCK1 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: RBCK1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RBCK1 were set to Polyglucosan body myopathy 1 with or without immunodeficiency 615895","entity_name":"RBCK1","entity_type":"gene"},{"created":"2020-01-14T13:20:49.862512+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PYGM was added\ngene: PYGM was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PYGM was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PYGM were set to Glycogen storage disease V McArdle disease 232600 AR","entity_name":"PYGM","entity_type":"gene"},{"created":"2020-01-14T13:20:49.788702+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PRKAG2 was added\ngene: PRKAG2 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PRKAG2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: PRKAG2 were set to Wolff-Parkinson-White syndrome        194200; Cardiomyopathy, hypertrophic 6        600858; Glycogen storage disease of heart, lethal congenital        261740","entity_name":"PRKAG2","entity_type":"gene"},{"created":"2020-01-14T13:20:49.715960+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: POLG2 was added\ngene: POLG2 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: POLG2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: POLG2 were set to Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4 610131","entity_name":"POLG2","entity_type":"gene"},{"created":"2020-01-14T13:20:49.642112+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: POLG was added\ngene: POLG was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: POLG was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: POLG were set to Mitochondrial DNA depletion syndrome 4B (MNGIE type) 613662; Mitochondrial recessive ataxia syndrome (includes SANDO and SCAE) 607459; Progressive external ophthalmoplegia, autosomal dominant 1 157640; Mitochondrial DNA depletion syndrome 4A (Alpers type) 203700; Progressive external ophthalmoplegia, autosomal recessive 1 258450","entity_name":"POLG","entity_type":"gene"},{"created":"2020-01-14T13:20:49.568589+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PHKB was added\ngene: PHKB was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PHKB was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PHKB were set to Phosphorylase kinase deficiency of liver and muscle, autosomal recessive 261750","entity_name":"PHKB","entity_type":"gene"},{"created":"2020-01-14T13:20:49.495162+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PHKA1 was added\ngene: PHKA1 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PHKA1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: PHKA1 were set to Muscle glycogenosis 300559","entity_name":"PHKA1","entity_type":"gene"},{"created":"2020-01-14T13:20:49.421991+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PGM1 was added\ngene: PGM1 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PGM1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PGM1 were set to Congenital disorder of glycosylation, type It 614921","entity_name":"PGM1","entity_type":"gene"},{"created":"2020-01-14T13:20:49.348366+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PGK1 was added\ngene: PGK1 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PGK1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: PGK1 were set to Phosphoglycerate kinase 1 deficiency 300653","entity_name":"PGK1","entity_type":"gene"},{"created":"2020-01-14T13:20:49.272847+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PGAM2 was added\ngene: PGAM2 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PGAM2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PGAM2 were set to Glycogen storage disease X 261670","entity_name":"PGAM2","entity_type":"gene"},{"created":"2020-01-14T13:20:49.197802+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PFKM was added\ngene: PFKM was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: PFKM was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: PFKM were set to Glycogen storage disease VII 232800","entity_name":"PFKM","entity_type":"gene"},{"created":"2020-01-14T13:20:49.124141+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: LPIN1 was added\ngene: LPIN1 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: LPIN1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: LPIN1 were set to Myoglobinuria, acute recurrent, autosomal recessive        268200","entity_name":"LPIN1","entity_type":"gene"},{"created":"2020-01-14T13:20:49.049964+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: LDHA was added\ngene: LDHA was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: LDHA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: LDHA were set to Glycogen storage disease XI        612933","entity_name":"LDHA","entity_type":"gene"},{"created":"2020-01-14T13:20:48.976545+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: LAMP2 was added\ngene: LAMP2 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: LAMP2 was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)\nPhenotypes for gene: LAMP2 were set to Danon disease 300257","entity_name":"LAMP2","entity_type":"gene"},{"created":"2020-01-14T13:20:48.903571+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ISCU was added\ngene: ISCU was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ISCU was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ISCU were set to Myopathy with lactic acidosis, hereditary 255125","entity_name":"ISCU","entity_type":"gene"},{"created":"2020-01-14T13:20:48.831294+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: HADHB was added\ngene: HADHB was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: HADHB was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HADHB were set to Trifunctional protein deficiency        609015","entity_name":"HADHB","entity_type":"gene"},{"created":"2020-01-14T13:20:48.758754+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: HADHA was added\ngene: HADHA was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: HADHA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HADHA were set to Trifunctional protein deficiency 609015","entity_name":"HADHA","entity_type":"gene"},{"created":"2020-01-14T13:20:48.687213+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: GYS1 was added\ngene: GYS1 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: GYS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GYS1 were set to Glycogen storage disease 0, muscle 611556","entity_name":"GYS1","entity_type":"gene"},{"created":"2020-01-14T13:20:48.616503+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: GYG1 was added\ngene: GYG1 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: GYG1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GYG1 were set to ?Glycogen storage disease XV 613507; Polyglucosan body myopathy 2 616199","entity_name":"GYG1","entity_type":"gene"},{"created":"2020-01-14T13:20:48.545550+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: GBE1 was added\ngene: GBE1 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: GBE1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GBE1 were set to Glycogen storage disease IV 232500","entity_name":"GBE1","entity_type":"gene"},{"created":"2020-01-14T13:20:48.474396+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: GAA was added\ngene: GAA was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: GAA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GAA were set to Glycogen storage disease II 232300","entity_name":"GAA","entity_type":"gene"},{"created":"2020-01-14T13:20:48.403822+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: FKTN was added\ngene: FKTN was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: FKTN was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: FKTN were set to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 253800; Fukuyama congenital muscular dystrophy","entity_name":"FKTN","entity_type":"gene"},{"created":"2020-01-14T13:20:48.334180+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: FKRP was added\ngene: FKRP was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: FKRP was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: FKRP were set to Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5 607155","entity_name":"FKRP","entity_type":"gene"},{"created":"2020-01-14T13:20:48.263188+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ETFDH was added\ngene: ETFDH was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ETFDH was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ETFDH were set to Glutaric acidemia IIC 231680","entity_name":"ETFDH","entity_type":"gene"},{"created":"2020-01-14T13:20:48.185115+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ETFB was added\ngene: ETFB was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ETFB was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ETFB were set to Glutaric acidemia IIB 231680","entity_name":"ETFB","entity_type":"gene"},{"created":"2020-01-14T13:20:48.114754+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ETFA was added\ngene: ETFA was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ETFA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ETFA were set to Glutaric acidemia IIA 231680","entity_name":"ETFA","entity_type":"gene"},{"created":"2020-01-14T13:20:48.043929+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ENO3 was added\ngene: ENO3 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ENO3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ENO3 were set to ?Glycogen storage disease XIII 612932","entity_name":"ENO3","entity_type":"gene"},{"created":"2020-01-14T13:20:47.969514+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: DYSF was added\ngene: DYSF was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: DYSF was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: DYSF were set to Muscular dystrophy, limb-girdle, type 2B 253601; Myopathy, distal, with anterior tibial onset  606768; Miyoshi muscular dystrophy 1 254130","entity_name":"DYSF","entity_type":"gene"},{"created":"2020-01-14T13:20:47.897197+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: DMD was added\ngene: DMD was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: DMD was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: DMD were set to Becker muscular dystrophy 300376","entity_name":"DMD","entity_type":"gene"},{"created":"2020-01-14T13:20:47.825003+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CYP2C8 was added\ngene: CYP2C8 was added to Rhabdomyolysis_RMH. Sources: Expert Review Red,Royal Melbourne Hospital\nMode of inheritance for gene: CYP2C8 was set to Unknown\nPhenotypes for gene: CYP2C8 were set to Rhabdomyolysis, cerivastatin-induced","entity_name":"CYP2C8","entity_type":"gene"},{"created":"2020-01-14T13:20:47.752438+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CPT2 was added\ngene: CPT2 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CPT2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CPT2 were set to CPT II deficiency, myopathic, stress-induced (exercise intolerance and rhabdomyolysis, late onset) 255110","entity_name":"CPT2","entity_type":"gene"},{"created":"2020-01-14T13:20:47.681797+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CAV3 was added\ngene: CAV3 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CAV3 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: CAV3 were set to Muscular dystrophy, limb-girdle, type IC 607801; Rippling muscle disease 606072; Myopathy, distal, Tateyama type 614321","entity_name":"CAV3","entity_type":"gene"},{"created":"2020-01-14T13:20:47.612154+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CACNA1S was added\ngene: CACNA1S was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CACNA1S was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: CACNA1S were set to {Malignant hyperthermia susceptibility 5}, 601887","entity_name":"CACNA1S","entity_type":"gene"},{"created":"2020-01-14T13:20:47.542551+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ANO5 was added\ngene: ANO5 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ANO5 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ANO5 were set to Miyoshi muscular dystrophy 3 613319; Muscular dystrophy, limb-girdle, type 2L 611307","entity_name":"ANO5","entity_type":"gene"},{"created":"2020-01-14T13:20:47.473338+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: AMPD1 was added\ngene: AMPD1 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: AMPD1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AMPD1 were set to Myopathy due to myoadenylate deaminase deficiency 615511; Rhabdomyolysis","entity_name":"AMPD1","entity_type":"gene"},{"created":"2020-01-14T13:20:47.403451+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ALDOA was added\ngene: ALDOA was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ALDOA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ALDOA were set to Glycogen storage disease XII 611881","entity_name":"ALDOA","entity_type":"gene"},{"created":"2020-01-14T13:20:47.334841+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: AGL was added\ngene: AGL was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: AGL was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AGL were set to Glycogen storage disease IIIa 232400; Glycogen storage disease IIIb 232400","entity_name":"AGL","entity_type":"gene"},{"created":"2020-01-14T13:20:47.265420+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ACADVL was added\ngene: ACADVL was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ACADVL was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ACADVL were set to VLCAD deficiency 201475","entity_name":"ACADVL","entity_type":"gene"},{"created":"2020-01-14T13:20:47.196160+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ACADM was added\ngene: ACADM was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ACADM was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ACADM were set to Acyl-CoA dehydrogenase, medium chain, deficiency of 201450; Rhabdomyolysis","entity_name":"ACADM","entity_type":"gene"},{"created":"2020-01-14T13:20:47.122999+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ACAD9 was added\ngene: ACAD9 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ACAD9 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ACAD9 were set to Mitochondrial complex I deficiency due to ACAD9 deficiency 611126","entity_name":"ACAD9","entity_type":"gene"},{"created":"2020-01-14T13:20:47.079167+11:00","panel_name":"Rhabdomyolysis_RMH","panel_id":3084,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"panel","text":"Added panel Rhabdomyolysis_RMH","entity_name":null,"entity_type":null},{"created":"2020-01-14T11:26:03.808455+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ITSN1 as ready","entity_name":"ITSN1","entity_type":"gene"},{"created":"2020-01-14T11:26:03.796456+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: itsn1 has been classified as Green List (High Evidence).","entity_name":"ITSN1","entity_type":"gene"},{"created":"2020-01-14T11:25:28.873100+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBC1D8B as ready","entity_name":"TBC1D8B","entity_type":"gene"},{"created":"2020-01-14T11:25:28.860740+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbc1d8b has been classified as Green List (High Evidence).","entity_name":"TBC1D8B","entity_type":"gene"},{"created":"2020-01-14T11:24:49.181773+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ANLN as ready","entity_name":"ANLN","entity_type":"gene"},{"created":"2020-01-14T11:24:49.170122+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: anln has been classified as Amber List (Moderate Evidence).","entity_name":"ANLN","entity_type":"gene"},{"created":"2020-01-14T11:24:42.195440+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ANLN were changed from Focal segmental glomerulosclerosis 8, OMIM #616032 to Focal segmental glomerulosclerosis 8, OMIM #616032","entity_name":"ANLN","entity_type":"gene"},{"created":"2020-01-14T11:24:09.817005+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ANLN were changed from  to Focal segmental glomerulosclerosis 8, OMIM #616032","entity_name":"ANLN","entity_type":"gene"},{"created":"2020-01-14T11:23:34.472552+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ANLN were set to ","entity_name":"ANLN","entity_type":"gene"},{"created":"2020-01-14T11:23:00.877660+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ANLN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ANLN","entity_type":"gene"},{"created":"2020-01-14T11:22:03.035414+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CD2AP as ready","entity_name":"CD2AP","entity_type":"gene"},{"created":"2020-01-14T11:22:03.022503+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd2ap has been classified as Amber List (Moderate Evidence).","entity_name":"CD2AP","entity_type":"gene"},{"created":"2020-01-14T11:21:55.658730+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CD2AP were changed from Glomerulosclerosis, focal segmental, 3, OMIM #607832 to Glomerulosclerosis, focal segmental, 3, OMIM #607832","entity_name":"CD2AP","entity_type":"gene"},{"created":"2020-01-14T11:21:13.111369+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CD2AP were changed from  to Glomerulosclerosis, focal segmental, 3, OMIM #607832","entity_name":"CD2AP","entity_type":"gene"},{"created":"2020-01-14T11:20:37.079812+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CD2AP were set to ","entity_name":"CD2AP","entity_type":"gene"},{"created":"2020-01-14T11:19:58.964524+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CD2AP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CD2AP","entity_type":"gene"},{"created":"2020-01-14T11:13:51.037225+11:00","panel_name":"Congenital Myaesthenic Syndrome_RMH","panel_id":3078,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: VAMP1 was added\ngene: VAMP1 was added to Congenital Myaesthenic Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: VAMP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: VAMP1 were set to presynaptic CMS; Congenital myasthenic syndrome","entity_name":"VAMP1","entity_type":"gene"},{"created":"2020-01-14T11:13:50.960061+11:00","panel_name":"Congenital Myaesthenic Syndrome_RMH","panel_id":3078,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: UNC13A was added\ngene: UNC13A was added to Congenital Myaesthenic Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Amber\nMode of inheritance for gene: UNC13A was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: UNC13A were set to 19558619; 27648472\nPhenotypes for gene: UNC13A were set to microcephaly, cortical hyperexcitability, and fatal myasthenia","entity_name":"UNC13A","entity_type":"gene"},{"created":"2020-01-14T11:13:50.882281+11:00","panel_name":"Congenital Myaesthenic Syndrome_RMH","panel_id":3078,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SYT2 was added\ngene: SYT2 was added to Congenital Myaesthenic Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: SYT2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SYT2 were set to Myasthenic syndrome, congenital, 7, presynaptic, 616040","entity_name":"SYT2","entity_type":"gene"},{"created":"2020-01-14T11:13:50.808308+11:00","panel_name":"Congenital Myaesthenic Syndrome_RMH","panel_id":3078,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: SNAP25 was added\ngene: SNAP25 was added to Congenital Myaesthenic Syndrome_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: SNAP25 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SNAP25 were set to ?Myasthenic syndrome, congenital, 18,  616330","entity_name":"SNAP25","entity_type":"gene"}]}