{"count":220504,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2029","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2027","results":[{"created":"2019-12-24T10:34:07.710122+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CWC27 was added\ngene: CWC27 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CWC27 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CWC27 were set to Retinitis pigmentosa with or without skeletal anomalies, 250410","entity_name":"CWC27","entity_type":"gene"},{"created":"2019-12-24T10:34:07.642296+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CRB1 was added\ngene: CRB1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\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":"2019-12-24T10:34:07.576323+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CNGB1 was added\ngene: CNGB1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CNGB1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CNGB1 were set to Retinitis pigmentosa 45, 613767","entity_name":"CNGB1","entity_type":"gene"},{"created":"2019-12-24T10:34:07.506481+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CNGA1 was added\ngene: CNGA1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CNGA1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: CNGA1 were set to Retinitis pigmentosa 49, 613756","entity_name":"CNGA1","entity_type":"gene"},{"created":"2019-12-24T10:34:07.435392+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CLRN1 was added\ngene: CLRN1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_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 Retinitis pigmentosa 61, 614180","entity_name":"CLRN1","entity_type":"gene"},{"created":"2019-12-24T10:34:07.367982+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CLN3 was added\ngene: CLN3 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CLN3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CLN3 were set to Retinitis pigmentosa; Juvenile neuronal ceroid lipofuscinosis","entity_name":"CLN3","entity_type":"gene"},{"created":"2019-12-24T10:34:07.300895+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CLCC1 was added\ngene: CLCC1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CLCC1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CLCC1 were set to 30157172\nPhenotypes for gene: CLCC1 were set to Retinitis pigmentosa 32","entity_name":"CLCC1","entity_type":"gene"},{"created":"2019-12-24T10:34:07.234626+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CHM was added\ngene: CHM was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CHM 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: CHM were set to Retinitis pigmentosa; Choroideremia (degeneration of the choriocapillaris, the retinal pigment epithelium, and the photoreceptor of the eye)","entity_name":"CHM","entity_type":"gene"},{"created":"2019-12-24T10:34:07.164091+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CERKL was added\ngene: CERKL was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\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":"2019-12-24T10:34:07.097611+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CEP290 was added\ngene: CEP290 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CEP290 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CEP290 were set to Senior-Loken syndrome 6, 610189; Meckel syndrome 4, 611134; Leber congenital amaurosis 10, 611755; Joubert syndrome 5, 610188; Bardet-Biedl syndrome 14, 209900","entity_name":"CEP290","entity_type":"gene"},{"created":"2019-12-24T10:34:07.031754+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: CDHR1 was added\ngene: CDHR1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: CDHR1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CDHR1 were set to Achromatopsia, Cone, and Cone-rod Dystrophy; Cone-Rod Dystrophy, Recessive; Retinitis pigmentosa 65; Cone-rod dystrophy 15, 613660","entity_name":"CDHR1","entity_type":"gene"},{"created":"2019-12-24T10:34:06.966368+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: C8orf37 was added\ngene: C8orf37 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: C8orf37 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: C8orf37 were set to Achromatopsia, Cone, and Cone-rod Dystrophy; Retinitis pigmentosa 64, 614500","entity_name":"C8orf37","entity_type":"gene"},{"created":"2019-12-24T10:34:06.901037+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: BEST1 was added\ngene: BEST1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: BEST1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: BEST1 were set to Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma, 1; Maculopathy, bull's-eye; Best Vitelliform Macular Dystrophy; Best macular dystrophy, 153700; Vitreoretinochoroidopathy, 193220; Retinitis pigmentosa; Retinitis Pigmentosa, Recessive; Bestrophinopathy, 611809; Vitelliform macular dystrophy, adult-onset, 608161","entity_name":"BEST1","entity_type":"gene"},{"created":"2019-12-24T10:34:06.837018+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: BBS2 was added\ngene: BBS2 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: BBS2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: BBS2 were set to Bardet-Biedl syndrome 2; Retinitis pigmentosa 74","entity_name":"BBS2","entity_type":"gene"},{"created":"2019-12-24T10:34:06.769521+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: BBS1 was added\ngene: BBS1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: BBS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: BBS1 were set to Retinitis pigmentosa","entity_name":"BBS1","entity_type":"gene"},{"created":"2019-12-24T10:34:06.701843+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ARL6 was added\ngene: ARL6 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ARL6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARL6 were set to Retinitis pigmentosa 55, 613575; Bardet-Biedl syndrome 3, 209900","entity_name":"ARL6","entity_type":"gene"},{"created":"2019-12-24T10:34:06.636453+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ARL2BP was added\ngene: ARL2BP was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ARL2BP was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARL2BP were set to Retinitis pigmentosa with or without situs inversus, 615434","entity_name":"ARL2BP","entity_type":"gene"},{"created":"2019-12-24T10:34:06.563817+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ARHGEF18 was added\ngene: ARHGEF18 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ARHGEF18 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ARHGEF18 were set to Retinitis pigmentosa 78 617433","entity_name":"ARHGEF18","entity_type":"gene"},{"created":"2019-12-24T10:34:06.494891+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: AIPL1 was added\ngene: AIPL1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: AIPL1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AIPL1 were set to Retinitis  pigmentosa, juvenile; Leber congenital  amaurosis 4; Cone-rod dystrophy","entity_name":"AIPL1","entity_type":"gene"},{"created":"2019-12-24T10:34:06.428062+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: AHR was added\ngene: AHR was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: AHR was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AHR were set to 29726989\nPhenotypes for gene: AHR were set to ?Retinitis pigmentosa 85","entity_name":"AHR","entity_type":"gene"},{"created":"2019-12-24T10:34:06.362949+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: AHI1 was added\ngene: AHI1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: AHI1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AHI1 were set to Joubert syndrome 17","entity_name":"AHI1","entity_type":"gene"},{"created":"2019-12-24T10:34:06.295028+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: AGBL5 was added\ngene: AGBL5 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: AGBL5 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: AGBL5 were set to Retinitis pigmentosa 75 617023","entity_name":"AGBL5","entity_type":"gene"},{"created":"2019-12-24T10:34:06.231216+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ADGRA3 was added\ngene: ADGRA3 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Red\nMode of inheritance for gene: ADGRA3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ADGRA3 were set to 23105016\nPhenotypes for gene: ADGRA3 were set to retinal dystrophy","entity_name":"ADGRA3","entity_type":"gene"},{"created":"2019-12-24T10:34:06.164647+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ABHD12 was added\ngene: ABHD12 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_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 andCataract (PHARC); Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract, 614857","entity_name":"ABHD12","entity_type":"gene"},{"created":"2019-12-24T10:34:06.101366+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ABCA4 was added\ngene: ABCA4 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ABCA4 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: ABCA4 were set to Macular Degeneration (Dominant); Stargardt disease 1, 248200; Macular degeneration, age-related, 2, 153800; Achromatopsia, Cone, and Cone-rod Dystrophy; Retinal dystrophy, early-onset severe, 248200; Stargardt Disease, Recessive; Retinitis pigmentosa 19, 601718; Cone-rod dystrophy 3, 604116; Macular Dystrophy/Degeneration/Stargardt Disease; Fundus flavimaculatus, 248200","entity_name":"ABCA4","entity_type":"gene"},{"created":"2019-12-24T10:34:05.960581+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ARL3 was added\ngene: ARL3 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green\nMode of inheritance for gene: ARL3 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: ARL3 were set to 26936825; 16565502; 26964041; 26814127; 30932721; 30269812\nPhenotypes for gene: ARL3 were set to Retinitis pigmentosa 83; Joubert syndrome 35","entity_name":"ARL3","entity_type":"gene"},{"created":"2019-12-24T10:34:05.892856+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"entity","text":"gene: ADIPOR1 was added\ngene: ADIPOR1 was added to Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH. Sources: Expert Review Amber,Royal Melbourne Hospital\nMode of inheritance for gene: ADIPOR1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: ADIPOR1 were set to 26662040; 25736573; 30254279; 27655171\nPhenotypes for gene: ADIPOR1 were set to syndromic retinitis pigmentosa; non-syndromic autosomal dominant retinitis pigmentosa","entity_name":"ADIPOR1","entity_type":"gene"},{"created":"2019-12-24T10:34:05.849428+11:00","panel_name":"Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","panel_id":277,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"panel","text":"Added panel Autosomal Recessive/X-Linked Retinitis Pigmentosa_RMH","entity_name":null,"entity_type":null},{"created":"2019-12-24T10:27:01.167488+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.414","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: INSRR as ready","entity_name":"INSRR","entity_type":"gene"},{"created":"2019-12-24T10:27:01.156202+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.414","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: insrr has been classified as Red List (Low Evidence).","entity_name":"INSRR","entity_type":"gene"},{"created":"2019-12-24T10:26:51.914075+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.414","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: INSRR as Red List (low evidence)","entity_name":"INSRR","entity_type":"gene"},{"created":"2019-12-24T10:26:51.909185+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.414","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment on list classification: Agreed, cannot find evidence for Mendelian gene-disease association.","entity_name":"INSRR","entity_type":"gene"},{"created":"2019-12-24T10:26:51.867063+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.414","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: insrr has been classified as Red List (Low Evidence).","entity_name":"INSRR","entity_type":"gene"},{"created":"2019-12-24T10:17:46.291675+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.413","user_name":"Lauren Akesson","item_type":"entity","text":"reviewed gene: INSRR: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"INSRR","entity_type":"gene"},{"created":"2019-12-24T10:09:57.324110+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.413","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GRIK5 as ready","entity_name":"GRIK5","entity_type":"gene"},{"created":"2019-12-24T10:09:57.313044+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.413","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: grik5 has been classified as Red List (Low Evidence).","entity_name":"GRIK5","entity_type":"gene"},{"created":"2019-12-24T10:09:45.231475+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.413","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GRIK5 as Red List (low evidence)","entity_name":"GRIK5","entity_type":"gene"},{"created":"2019-12-24T10:09:45.220445+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.413","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment on list classification: Agreed, cannot find evidence for Mendelian gene-disease association.","entity_name":"GRIK5","entity_type":"gene"},{"created":"2019-12-24T10:09:44.976009+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.413","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: grik5 has been classified as Red List (Low Evidence).","entity_name":"GRIK5","entity_type":"gene"},{"created":"2019-12-24T10:03:18.767355+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.412","user_name":"Crystle Lee","item_type":"entity","text":"reviewed gene: GRIK5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"GRIK5","entity_type":"gene"},{"created":"2019-12-24T09:20:57.186949+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAGI2 as ready","entity_name":"MAGI2","entity_type":"gene"},{"created":"2019-12-24T09:20:57.176145+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: magi2 has been classified as Green List (High Evidence).","entity_name":"MAGI2","entity_type":"gene"},{"created":"2019-12-24T09:20:53.590026+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAGI2 were changed from  to Nephrotic syndrome, type 15, MIM# 617609","entity_name":"MAGI2","entity_type":"gene"},{"created":"2019-12-24T09:20:28.021531+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MAGI2 were set to ","entity_name":"MAGI2","entity_type":"gene"},{"created":"2019-12-24T09:19:58.070214+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MAGI2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MAGI2","entity_type":"gene"},{"created":"2019-12-24T09:19:25.372357+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MAGI2: Rating: GREEN; Mode of pathogenicity: None; Publications: 27932480, 25271328, 25108225; Phenotypes: Nephrotic syndrome, type 15, MIM# 617609; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MAGI2","entity_type":"gene"},{"created":"2019-12-23T18:30:07.543461+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CD151 as ready","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:30:07.532570+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd151 has been classified as Green List (High Evidence).","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:30:01.421379+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CD151 as Green List (high evidence)","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:30:01.402584+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd151 has been classified as Green List (High Evidence).","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:29:27.812142+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CD151 was added\ngene: CD151 was added to Deafness_MelbourneGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: CD151 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CD151 were set to 15265795; 29138120\nPhenotypes for gene: CD151 were set to Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057\nReview for gene: CD151 was set to GREEN\nAdded comment: Three families described in the literature. \nSources: Literature","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:27:27.214532+11:00","panel_name":"Epidermolysis bullosa_VCGS","panel_id":101,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CD151 as ready","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:27:27.203698+11:00","panel_name":"Epidermolysis bullosa_VCGS","panel_id":101,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd151 has been classified as Green List (High Evidence).","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:27:22.053159+11:00","panel_name":"Epidermolysis bullosa_VCGS","panel_id":101,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CD151 as Green List (high evidence)","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:27:22.042396+11:00","panel_name":"Epidermolysis bullosa_VCGS","panel_id":101,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd151 has been classified as Green List (High Evidence).","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:26:40.571617+11:00","panel_name":"Epidermolysis bullosa_VCGS","panel_id":101,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CD151 was added\ngene: CD151 was added to Epidermolysis bullosa_VCGS. Sources: Literature\nMode of inheritance for gene: CD151 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CD151 were set to 15265795; 29138120\nPhenotypes for gene: CD151 were set to Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057\nAdded comment: Three families described in the literature \nSources: Literature","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:25:00.582101+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CD151 as ready","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:25:00.570648+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd151 has been classified as Green List (High Evidence).","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:24:56.131430+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CD151 as Green List (high evidence)","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:24:56.117697+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd151 has been classified as Green List (High Evidence).","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:24:27.408347+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CD151 was added\ngene: CD151 was added to Proteinuria_VCGS_KidGen. Sources: Expert list\nMode of inheritance for gene: CD151 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CD151 were set to 15265795; 29138120\nPhenotypes for gene: CD151 were set to Nephropathy with pretibial epidermolysis bullosa and deafness, MIM#609057\nReview for gene: CD151 was set to GREEN\nAdded comment: Three families described in the literature. \nSources: Expert list","entity_name":"CD151","entity_type":"gene"},{"created":"2019-12-23T18:00:59.945337+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAN1 as ready","entity_name":"FAN1","entity_type":"gene"},{"created":"2019-12-23T18:00:59.934877+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fan1 has been classified as Green List (High Evidence).","entity_name":"FAN1","entity_type":"gene"},{"created":"2019-12-23T18:00:51.863147+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FAN1 as Green List (high evidence)","entity_name":"FAN1","entity_type":"gene"},{"created":"2019-12-23T18:00:51.850152+11:00","panel_name":"Renal ciliopathies and nephronophthisis_KidGen_VCGS","panel_id":193,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fan1 has been classified as Green List (High Evidence).","entity_name":"FAN1","entity_type":"gene"},{"created":"2019-12-23T16:04:42.735280+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.412","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBC1D8B as ready","entity_name":"TBC1D8B","entity_type":"gene"},{"created":"2019-12-23T16:04:42.727584+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.412","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":"2019-12-23T16:04:21.763008+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.412","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBC1D8B were changed from  to Nephrotic syndrome, type 20, MIM# 301028","entity_name":"TBC1D8B","entity_type":"gene"},{"created":"2019-12-23T16:04:08.496383+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.411","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBC1D8B were set to ","entity_name":"TBC1D8B","entity_type":"gene"},{"created":"2019-12-23T16:03:50.057407+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.410","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MPST as ready","entity_name":"MPST","entity_type":"gene"},{"created":"2019-12-23T16:03:50.050826+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.410","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mpst has been classified as Red List (Low Evidence).","entity_name":"MPST","entity_type":"gene"},{"created":"2019-12-23T16:03:39.540758+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.410","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MPST as Red List (low evidence)","entity_name":"MPST","entity_type":"gene"},{"created":"2019-12-23T16:03:39.533667+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.410","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mpst has been classified as Red List (Low Evidence).","entity_name":"MPST","entity_type":"gene"},{"created":"2019-12-23T16:02:42.183221+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.409","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: MPST: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"MPST","entity_type":"gene"},{"created":"2019-12-23T16:02:33.595937+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.409","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBC1D8B was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"TBC1D8B","entity_type":"gene"},{"created":"2019-12-23T16:02:14.732025+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.408","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TBC1D8B: Rating: GREEN; Mode of pathogenicity: None; Publications: 30661770; Phenotypes: Nephrotic syndrome, type 20, MIM# 301028; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"TBC1D8B","entity_type":"gene"},{"created":"2019-12-23T16:00:48.230621+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBC1D8B were changed from  to Nephrotic syndrome, type 20, MIM# 301028","entity_name":"TBC1D8B","entity_type":"gene"},{"created":"2019-12-23T16:00:23.583917+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBC1D8B were set to ","entity_name":"TBC1D8B","entity_type":"gene"},{"created":"2019-12-23T15:59:57.908917+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBC1D8B was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"TBC1D8B","entity_type":"gene"},{"created":"2019-12-23T15:59:11.908183+11:00","panel_name":"Proteinuria_VCGS_KidGen","panel_id":144,"panel_version":"0.54","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: TBC1D8B: Rating: GREEN; Mode of pathogenicity: None; Publications: 30661770; Phenotypes: Nephrotic syndrome, type 20, MIM# 301028; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"TBC1D8B","entity_type":"gene"},{"created":"2019-12-23T15:55:37.554121+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.408","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ANKRD17 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ANKRD17","entity_type":"gene"},{"created":"2019-12-23T15:54:40.190296+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.407","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRIM24 as ready","entity_name":"TRIM24","entity_type":"gene"},{"created":"2019-12-23T15:54:40.181848+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.407","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trim24 has been classified as Red List (Low Evidence).","entity_name":"TRIM24","entity_type":"gene"},{"created":"2019-12-23T15:54:29.310097+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.407","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRIM24 as Red List (low evidence)","entity_name":"TRIM24","entity_type":"gene"},{"created":"2019-12-23T15:54:29.302197+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.407","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trim24 has been classified as Red List (Low Evidence).","entity_name":"TRIM24","entity_type":"gene"},{"created":"2019-12-23T15:53:33.356226+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.406","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: TRIM24: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TRIM24","entity_type":"gene"},{"created":"2019-12-23T15:50:04.195085+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.406","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARID5B as ready","entity_name":"ARID5B","entity_type":"gene"},{"created":"2019-12-23T15:50:04.188210+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.406","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arid5b has been classified as Red List (Low Evidence).","entity_name":"ARID5B","entity_type":"gene"},{"created":"2019-12-23T15:49:55.250429+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.406","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ARID5B as Red List (low evidence)","entity_name":"ARID5B","entity_type":"gene"},{"created":"2019-12-23T15:49:55.243101+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.406","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arid5b has been classified as Red List (Low Evidence).","entity_name":"ARID5B","entity_type":"gene"},{"created":"2019-12-23T15:49:18.222952+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.405","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: ARID5B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"ARID5B","entity_type":"gene"},{"created":"2019-12-23T15:46:13.583639+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.405","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MLX as ready","entity_name":"MLX","entity_type":"gene"},{"created":"2019-12-23T15:46:13.576929+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.405","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mlx has been classified as Red List (Low Evidence).","entity_name":"MLX","entity_type":"gene"},{"created":"2019-12-23T15:46:03.189875+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.405","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MLX as Red List (low evidence)","entity_name":"MLX","entity_type":"gene"},{"created":"2019-12-23T15:46:03.181120+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.405","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mlx has been classified as Red List (Low Evidence).","entity_name":"MLX","entity_type":"gene"},{"created":"2019-12-23T15:45:27.877849+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.404","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: MLX: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"MLX","entity_type":"gene"},{"created":"2019-12-23T15:42:12.636127+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.404","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: REV3L as ready","entity_name":"REV3L","entity_type":"gene"},{"created":"2019-12-23T15:42:12.629068+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.404","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rev3l has been classified as Green List (High Evidence).","entity_name":"REV3L","entity_type":"gene"},{"created":"2019-12-23T15:42:04.236948+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.404","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: REV3L were changed from  to Moebius syndrome","entity_name":"REV3L","entity_type":"gene"},{"created":"2019-12-23T15:41:49.478604+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.403","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: REV3L were set to ","entity_name":"REV3L","entity_type":"gene"}]}