{"count":220725,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2021","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2019","results":[{"created":"2019-12-31T10:50:36.986471+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CACNA1D were changed from  to Sinoatrial node dysfunction and deafness, MIM# 614896","entity_name":"CACNA1D","entity_type":"gene"},{"created":"2019-12-31T10:50:16.505356+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CACNA1D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CACNA1D","entity_type":"gene"},{"created":"2019-12-31T10:49:51.396747+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CACNA1D were set to ","entity_name":"CACNA1D","entity_type":"gene"},{"created":"2019-12-31T10:49:27.887383+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CACNA1D as Amber List (moderate evidence)","entity_name":"CACNA1D","entity_type":"gene"},{"created":"2019-12-31T10:49:27.876012+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cacna1d has been classified as Amber List (Moderate Evidence).","entity_name":"CACNA1D","entity_type":"gene"},{"created":"2019-12-31T10:48:58.347183+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CACNA1D: Rating: AMBER; Mode of pathogenicity: None; Publications: 21131953, 15357422, 22678062; Phenotypes: Sinoatrial node dysfunction and deafness, MIM# 614896; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CACNA1D","entity_type":"gene"},{"created":"2019-12-31T10:48:35.463434+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.23","user_name":"Lilian Rudd","item_type":"entity","text":"reviewed gene: BDP1: Rating: RED; Mode of pathogenicity: None; Publications: 24312468, 25060281; Phenotypes: Non syndromic hearing loss; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T10:47:11.113763+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PITPNM3 was added\ngene: PITPNM3 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: PITPNM3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: PITPNM3 were set to 17377520; 22405330\nPhenotypes for gene: PITPNM3 were set to Cone-rod dystrophy 5, 600977","entity_name":"PITPNM3","entity_type":"gene"},{"created":"2019-12-31T10:47:11.035854+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ZFYVE26 was added\ngene: ZFYVE26 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: ZFYVE26 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ZFYVE26 were set to Recessive spastic paraplegia with retinal degeneration","entity_name":"ZFYVE26","entity_type":"gene"},{"created":"2019-12-31T10:47:10.956995+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: TIMP3 was added\ngene: TIMP3 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: TIMP3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TIMP3 were set to Sorsby fundus dystrophy","entity_name":"TIMP3","entity_type":"gene"},{"created":"2019-12-31T10:47:10.880285+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RS1 was added\ngene: RS1 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: RS1 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: RS1 were set to Developmental macular and foveal dystrophy (males with foveal schisis)","entity_name":"RS1","entity_type":"gene"},{"created":"2019-12-31T10:47:10.803205+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RPGRIP1 was added\ngene: RPGRIP1 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: RPGRIP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RPGRIP1 were set to Leber congenital amaurosis 6, 613826; Cone-rod dystrophy 13, 608194","entity_name":"RPGRIP1","entity_type":"gene"},{"created":"2019-12-31T10:47:10.725964+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RPGR was added\ngene: RPGR was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: RPGR 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: RPGR were set to Retinitis pigmentosa 3, 300029; Retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without deafness, 300455; Macular degeneration, X-linked atrophic, 300834; Cone-rod dystrophy, X-linked, 1, 304020","entity_name":"RPGR","entity_type":"gene"},{"created":"2019-12-31T10:47:10.648933+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RP1L1 was added\ngene: RP1L1 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: RP1L1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RP1L1 were set to Occult macular dystrophy, 613587","entity_name":"RP1L1","entity_type":"gene"},{"created":"2019-12-31T10:47:10.573084+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RLBP1 was added\ngene: RLBP1 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: RLBP1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: RLBP1 were set to Fundus  albipunctatus; Newfoundland rod - cone dystrophy; Fundus albipunctatus, 136880; Bothnia retinal  dystrophy; Retinitis punctata  albescens","entity_name":"RLBP1","entity_type":"gene"},{"created":"2019-12-31T10:47:10.498005+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RDH12 was added\ngene: RDH12 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: RDH12 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: RDH12 were set to Leber congenital amaurosis 13, 612712","entity_name":"RDH12","entity_type":"gene"},{"created":"2019-12-31T10:47:10.421947+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: RBP3 was added\ngene: RBP3 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Red,Royal Melbourne Hospital\nMode of inheritance for gene: RBP3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: RBP3 were set to ?Retinitis pigmentosa 66, 615233","entity_name":"RBP3","entity_type":"gene"},{"created":"2019-12-31T10:47:10.345810+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PRPH2 was added\ngene: PRPH2 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: PRPH2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: PRPH2 were set to Leber congenital amaurosis 18, MIM#608133; Macular dystrophy, vitelliform, 3, MIM#608161; Retinitis pigmentosa 7 and digenic form, MIM#608133; Choroidal dystrophy, central areolar 2, MIM#613105; Macular dystrophy, patterned, 1, MIM#169150; Retinitis punctata albescens, MIM#136880","entity_name":"PRPH2","entity_type":"gene"},{"created":"2019-12-31T10:47:10.261078+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PROM1 was added\ngene: PROM1 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: PROM1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: PROM1 were set to Retinitis pigmentosa 41, 612095; Cone-rod dystrophy 12, 612657; Stargardt disease 4, 603786; Macular dystrophy, retinal, 2, 608051","entity_name":"PROM1","entity_type":"gene"},{"created":"2019-12-31T10:47:10.173686+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: PRDM13 was added\ngene: PRDM13 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Amber,Royal Melbourne Hospital\nMode of inheritance for gene: PRDM13 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: PRDM13 were set to 29258872; 28973654; 26507665\nPhenotypes for gene: PRDM13 were set to Macular dystrophy, North Carolina type, MIM#136550","entity_name":"PRDM13","entity_type":"gene"},{"created":"2019-12-31T10:47:10.096256+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: OTX2 was added\ngene: OTX2 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: OTX2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: OTX2 were set to autosomal-dominant pattern dystrophy of the retinal pigment epithelium; early onset retinal dystrophy; Microphthalmia, syndromic 5, 610125","entity_name":"OTX2","entity_type":"gene"},{"created":"2019-12-31T10:47:09.944085+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: MFSD8 was added\ngene: MFSD8 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: MFSD8 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: MFSD8 were set to Ceroid lipofuscinosis, neuronal, 7, 610951; Macular dystrophy with central cone involvement, 616170","entity_name":"MFSD8","entity_type":"gene"},{"created":"2019-12-31T10:47:09.868470+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: IMPG2 was added\ngene: IMPG2 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: IMPG2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: IMPG2 were set to Retinitis  pigmentosa 56; Maculopathy,  IMPG2 - related","entity_name":"IMPG2","entity_type":"gene"},{"created":"2019-12-31T10:47:09.776746+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: IMPG1 was added\ngene: IMPG1 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: IMPG1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: IMPG1 were set to Macular dystrophy, vitelliform, 4","entity_name":"IMPG1","entity_type":"gene"},{"created":"2019-12-31T10:47:09.699180+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: HMCN1 was added\ngene: HMCN1 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: HMCN1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: HMCN1 were set to Macular Degeneration","entity_name":"HMCN1","entity_type":"gene"},{"created":"2019-12-31T10:47:09.618751+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: GUCA1B was added\ngene: GUCA1B was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: GUCA1B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: GUCA1B were set to Retinitis pigmentosa 48, 613827","entity_name":"GUCA1B","entity_type":"gene"},{"created":"2019-12-31T10:47:09.541426+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: FSCN2 was added\ngene: FSCN2 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: FSCN2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: FSCN2 were set to Retinitis pigmentosa 30, 607921","entity_name":"FSCN2","entity_type":"gene"},{"created":"2019-12-31T10:47:09.466639+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ELOVL4 was added\ngene: ELOVL4 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: ELOVL4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: ELOVL4 were set to Macular dystrophy, autosomal dominant, chromosome 6-linked, 600110; Stargardt disease 3, 600110; Ichthyosis, spastic quadriplegia, and mental retardation, 614457","entity_name":"ELOVL4","entity_type":"gene"},{"created":"2019-12-31T10:47:09.393980+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: EFEMP1 was added\ngene: EFEMP1 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: EFEMP1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: EFEMP1 were set to Inherited macular dystrophy (Doyne/dominant drusen)","entity_name":"EFEMP1","entity_type":"gene"},{"created":"2019-12-31T10:47:09.321073+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: DRAM2 was added\ngene: DRAM2 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: DRAM2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: DRAM2 were set to Cone-rod dystrophy 21, MIM#616502","entity_name":"DRAM2","entity_type":"gene"},{"created":"2019-12-31T10:47:09.247826+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CTNNA1 was added\ngene: CTNNA1 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: CTNNA1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: CTNNA1 were set to Macular dystrophy, butterfly-shaped pigmentary, 2, MIM#608970","entity_name":"CTNNA1","entity_type":"gene"},{"created":"2019-12-31T10:47:09.172220+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CRB1 was added\ngene: CRB1 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: CRB1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CRB1 were set to Pigmented paravenous chorioretinal atrophy, 172870; Leber congenital amaurosis 8, 613835; Retinitis pigmentosa-12, autosomal recessive, 600105","entity_name":"CRB1","entity_type":"gene"},{"created":"2019-12-31T10:47:09.093793+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CNGB3 was added\ngene: CNGB3 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: CNGB3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CNGB3 were set to Macular degeneration, juvenile, 248200 -3; Achromatopsia-3, 262300; Stargardt Disease, Recessive","entity_name":"CNGB3","entity_type":"gene"},{"created":"2019-12-31T10:47:08.945435+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CFH was added\ngene: CFH was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Amber,Royal Melbourne Hospital\nMode of inheritance for gene: CFH was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: CFH were set to {Macular degeneration, age-related, 4} 610698; Basal laminar drusen, 126700","entity_name":"CFH","entity_type":"gene"},{"created":"2019-12-31T10:47:08.872137+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CERKL was added\ngene: CERKL was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: CERKL was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CERKL were set to Retinitis pigmentosa 26, 608380","entity_name":"CERKL","entity_type":"gene"},{"created":"2019-12-31T10:47:08.796603+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CDH3 was added\ngene: CDH3 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: CDH3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CDH3 were set to Ectodermal dysplasia, ectrodactyly, and macular dystrophy, 225280; Hypotrichosis, congenital, with juvenile macular dystrophy, 601553","entity_name":"CDH3","entity_type":"gene"},{"created":"2019-12-31T10:47:08.721949+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: C1QTNF5 was added\ngene: C1QTNF5 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: C1QTNF5 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: C1QTNF5 were set to Retinal degeneration, late-onset, autosomal dominant, 605670; Retinitis pigmentosa","entity_name":"C1QTNF5","entity_type":"gene"},{"created":"2019-12-31T10:47:08.646295+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: BEST1 was added\ngene: BEST1 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: BEST1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: BEST1 were set to Best macular dystrophy, 153700; Vitelliform macular dystrophy, adult-onset, 608161; Vitreoretinochoroidopathy, 193220; Bestrophinopathy, 611809; Maculopathy, bull's-eye; Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma, 1","entity_name":"BEST1","entity_type":"gene"},{"created":"2019-12-31T10:47:08.570269+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ABCA4 was added\ngene: ABCA4 was added to Macular Dystrophy/Stargardt Disease_RMH. Sources: Expert Review Green,Royal Melbourne Hospital\nMode of inheritance for gene: ABCA4 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ABCA4 were set to Retinitis pigmentosa 19, 601718; Fundus flavimaculatus, 248200; Retinal dystrophy, early-onset severe, 248200; Macular degeneration, age-related, 2, 153800; Cone-rod dystrophy 3, 604116; Stargardt disease 1, 248200","entity_name":"ABCA4","entity_type":"gene"},{"created":"2019-12-31T10:47:08.521497+11:00","panel_name":"Macular Dystrophy/Stargardt Disease_RMH","panel_id":303,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"panel","text":"Added panel Macular Dystrophy/Stargardt Disease_RMH","entity_name":null,"entity_type":null},{"created":"2019-12-31T10:45:11.909535+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CABP2 as ready","entity_name":"CABP2","entity_type":"gene"},{"created":"2019-12-31T10:45:11.897855+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cabp2 has been classified as Green List (High Evidence).","entity_name":"CABP2","entity_type":"gene"},{"created":"2019-12-31T10:45:09.493376+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CABP2 were changed from  to Deafness, autosomal recessive 93, MIM# 614899","entity_name":"CABP2","entity_type":"gene"},{"created":"2019-12-31T10:44:44.166079+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CABP2 were set to ","entity_name":"CABP2","entity_type":"gene"},{"created":"2019-12-31T10:44:20.591052+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CABP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CABP2","entity_type":"gene"},{"created":"2019-12-31T10:43:50.928240+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CABP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 22981119, 31661684, 28183797; Phenotypes: Deafness, autosomal recessive 93, MIM# 614899; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CABP2","entity_type":"gene"},{"created":"2019-12-31T10:39:32.179423+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADCY1 as ready","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T10:39:32.167383+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adcy1 has been classified as Red List (Low Evidence).","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T10:39:29.522401+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ADCY1 were changed from Deafness, autosomal recessive 44, MIM# 610154 to Deafness, autosomal recessive 44, MIM# 610154","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T10:38:41.245740+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ADCY1 were changed from  to Deafness, autosomal recessive 44, MIM# 610154","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T10:38:21.281344+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ADCY1 were set to ","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T10:37:32.002163+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ADCY1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T10:37:03.983600+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ADCY1 as Red List (low evidence)","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T10:37:03.970561+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adcy1 has been classified as Red List (Low Evidence).","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T10:36:35.585128+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ADCY1: Rating: RED; Mode of pathogenicity: None; Publications: 24482543; Phenotypes: Deafness, autosomal recessive 44, MIM# 610154; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T10:32:39.357369+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ACTB were changed from Baraitser-Winter syndrome; Deafness-dystonia syndrome to Baraitser-Winter syndrome; Deafness-dystonia syndrome","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-31T10:32:21.825872+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACTB as ready","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-31T10:32:21.811978+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: actb has been classified as Green List (High Evidence).","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-31T10:32:14.687114+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ACTB were changed from  to Baraitser-Winter syndrome; Deafness-dystonia syndrome","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-31T10:31:37.951158+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ACTB were set to ","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-31T10:31:13.515478+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: ACTB was changed from  to Other","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-31T10:30:43.181544+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ACTB was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ACTB","entity_type":"gene"},{"created":"2019-12-31T10:22:02.803842+11:00","panel_name":"Autism_VCGS","panel_id":51,"panel_version":"0.18","user_name":"Seb L","item_type":"entity","text":"gene: SHANK1 was added\ngene: SHANK1 was added to Autism_VCGS. Sources: Literature\nMode of inheritance for gene: SHANK1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: SHANK1 were set to 25188300; 22503632\nPenetrance for gene: SHANK1 were set to unknown\nReview for gene: SHANK1 was set to GREEN\nAdded comment: SHANK1 missense and deletion variants have been described in multiple male patients (>10) with autism spectrum disorder. Several of the patients analysed in detail had normal intellect using various different IQ tests, with mild to moderately severe ADI-R scores for social, verbal, non-verbal and repetitive behaviour (Leblond et al 2014). \nSources: Literature","entity_name":"SHANK1","entity_type":"gene"},{"created":"2019-12-31T10:19:55.504113+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1450","user_name":"Seb L","item_type":"entity","text":"reviewed gene: SHANK1: Rating: RED; Mode of pathogenicity: None; Publications: 22503632, 25188300; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","entity_name":"SHANK1","entity_type":"gene"},{"created":"2019-12-31T10:00:46.635889+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRB2 as ready","entity_name":"CRB2","entity_type":"gene"},{"created":"2019-12-31T10:00:46.623606+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crb2 has been classified as Green List (High Evidence).","entity_name":"CRB2","entity_type":"gene"},{"created":"2019-12-31T10:00:44.240999+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CRB2 as Green List (high evidence)","entity_name":"CRB2","entity_type":"gene"},{"created":"2019-12-31T10:00:44.228668+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crb2 has been classified as Green List (High Evidence).","entity_name":"CRB2","entity_type":"gene"},{"created":"2019-12-31T10:00:34.534690+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CRB2 was added\ngene: CRB2 was added to Renal ciliopathies and nephronophthisis_KidGen_VCGS. Sources: Expert list\nMode of inheritance for gene: CRB2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CRB2 were set to 25557780\nPhenotypes for gene: CRB2 were set to Ventriculomegaly with cystic kidney disease, MIM#\t219730\nReview for gene: CRB2 was set to GREEN\nAdded comment: Three unrelated families described. \nSources: Expert list","entity_name":"CRB2","entity_type":"gene"},{"created":"2019-12-31T09:58:05.046976+11:00","panel_name":"Renal macrocystic disease_KidGen_VCGS","panel_id":194,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL4A1 as ready","entity_name":"COL4A1","entity_type":"gene"},{"created":"2019-12-31T09:58:05.001326+11:00","panel_name":"Renal macrocystic disease_KidGen_VCGS","panel_id":194,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col4a1 has been classified as Green List (High Evidence).","entity_name":"COL4A1","entity_type":"gene"},{"created":"2019-12-31T09:58:01.944868+11:00","panel_name":"Renal macrocystic disease_KidGen_VCGS","panel_id":194,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COL4A1 as Green List (high evidence)","entity_name":"COL4A1","entity_type":"gene"},{"created":"2019-12-31T09:58:01.933957+11:00","panel_name":"Renal macrocystic disease_KidGen_VCGS","panel_id":194,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col4a1 has been classified as Green List (High Evidence).","entity_name":"COL4A1","entity_type":"gene"},{"created":"2019-12-31T09:57:51.959627+11:00","panel_name":"Renal macrocystic disease_KidGen_VCGS","panel_id":194,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"gene: COL4A1 was added\ngene: COL4A1 was added to Renal macrocystic disease_KidGen_VCGS. Sources: Expert list\nMode of inheritance for gene: COL4A1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: COL4A1 were set to 25719457; 15882279\nPhenotypes for gene: COL4A1 were set to Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps, MIM#\t611773\nReview for gene: COL4A1 was set to GREEN\nAdded comment: Large renal cysts described in multiple individuals with this condition. \nSources: Expert list","entity_name":"COL4A1","entity_type":"gene"},{"created":"2019-12-31T09:53:07.213848+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP120 as ready","entity_name":"CEP120","entity_type":"gene"},{"created":"2019-12-31T09:53:07.197345+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep120 has been classified as Green List (High Evidence).","entity_name":"CEP120","entity_type":"gene"},{"created":"2019-12-31T09:52:57.134903+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CEP120 were changed from  to Short-rib thoracic dysplasia 13 with or without polydactyly, MIM# 616300","entity_name":"CEP120","entity_type":"gene"},{"created":"2019-12-31T09:52:44.177889+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CEP120 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP120","entity_type":"gene"},{"created":"2019-12-31T09:52:33.153808+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CEP120: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Short-rib thoracic dysplasia 13 with or without polydactyly, MIM# 616300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP120","entity_type":"gene"},{"created":"2019-12-31T09:48:58.637498+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C5orf42 as ready","entity_name":"C5orf42","entity_type":"gene"},{"created":"2019-12-31T09:48:58.625891+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c5orf42 has been classified as Red List (Low Evidence).","entity_name":"C5orf42","entity_type":"gene"},{"created":"2019-12-31T09:48:56.325933+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C5orf42 were changed from  to Joubert syndrome 17, MIM#614615; Orofaciodigital syndrome VI, MIM# 277170","entity_name":"C5orf42","entity_type":"gene"},{"created":"2019-12-31T09:48:44.710674+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C5orf42 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"C5orf42","entity_type":"gene"},{"created":"2019-12-31T09:48:35.590328+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: C5orf42 as Red List (low evidence)","entity_name":"C5orf42","entity_type":"gene"},{"created":"2019-12-31T09:48:35.577679+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c5orf42 has been classified as Red List (Low Evidence).","entity_name":"C5orf42","entity_type":"gene"},{"created":"2019-12-31T09:48:25.955738+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: C5orf42: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Joubert syndrome 17, MIM#614615, Orofaciodigital syndrome VI, MIM# 277170; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"C5orf42","entity_type":"gene"},{"created":"2019-12-31T09:42:46.303574+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: C2CD3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Orofaciodigital syndrome XIV, MIM# 615948; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"C2CD3","entity_type":"gene"},{"created":"2019-12-31T09:39:52.324439+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBIP1 as ready","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-31T09:39:52.312311+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbip1 has been classified as Amber List (Moderate Evidence).","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-31T09:39:49.421056+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBIP1 were changed from  to Bardet-Biedl syndrome 18, MIM#615995","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-31T09:39:45.304593+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBIP1 were set to ","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-31T09:39:22.493254+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBIP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-31T09:39:13.012942+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BBIP1 as Amber List (moderate evidence)","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-31T09:39:13.002104+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbip1 has been classified as Amber List (Moderate Evidence).","entity_name":"BBIP1","entity_type":"gene"},{"created":"2019-12-31T09:38:29.887060+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATXN10 as ready","entity_name":"ATXN10","entity_type":"gene"},{"created":"2019-12-31T09:38:29.874636+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atxn10 has been classified as Red List (Low Evidence).","entity_name":"ATXN10","entity_type":"gene"},{"created":"2019-12-31T09:38:27.373993+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ATXN10 were changed from  to Nephronophthisis","entity_name":"ATXN10","entity_type":"gene"},{"created":"2019-12-31T09:38:23.489230+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ATXN10 were set to ","entity_name":"ATXN10","entity_type":"gene"},{"created":"2019-12-31T09:38:01.299599+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ATXN10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ATXN10","entity_type":"gene"},{"created":"2019-12-31T09:37:51.886382+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ATXN10 as Red List (low evidence)","entity_name":"ATXN10","entity_type":"gene"}]}