{"count":220725,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2013","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2011","results":[{"created":"2020-01-02T20:50:07.395192+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1461","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PPP1R12A as Green List (high evidence)","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:50:07.383688+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1461","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppp1r12a has been classified as Green List (High Evidence).","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:49:40.213671+11:00","panel_name":"Holoprosencephaly and septo-optic dysplasia_VCGS","panel_id":112,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PPP1R12A as ready","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:49:40.201731+11:00","panel_name":"Holoprosencephaly and septo-optic dysplasia_VCGS","panel_id":112,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppp1r12a has been classified as Green List (High Evidence).","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:49:36.589047+11:00","panel_name":"Holoprosencephaly and septo-optic dysplasia_VCGS","panel_id":112,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PPP1R12A were set to ","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:49:04.086746+11:00","panel_name":"Holoprosencephaly and septo-optic dysplasia_VCGS","panel_id":112,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PPP1R12A as Green List (high evidence)","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:49:04.075921+11:00","panel_name":"Holoprosencephaly and septo-optic dysplasia_VCGS","panel_id":112,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppp1r12a has been classified as Green List (High Evidence).","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:48:18.912037+11:00","panel_name":"Disorders of Sex Differentiation_VCGS","panel_id":99,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PPP1R12A as ready","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:48:18.907047+11:00","panel_name":"Disorders of Sex Differentiation_VCGS","panel_id":99,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Now published; 12 individuals, upgraded to Green.","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:48:18.879936+11:00","panel_name":"Disorders of Sex Differentiation_VCGS","panel_id":99,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppp1r12a has been classified as Green List (High Evidence).","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:47:50.415644+11:00","panel_name":"Disorders of Sex Differentiation_VCGS","panel_id":99,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PPP1R12A as Green List (high evidence)","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:47:50.403348+11:00","panel_name":"Disorders of Sex Differentiation_VCGS","panel_id":99,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppp1r12a has been classified as Green List (High Evidence).","entity_name":"PPP1R12A","entity_type":"gene"},{"created":"2020-01-02T20:46:37.999492+11:00","panel_name":"Hypertrophic cardiomyopathy_VCGS","panel_id":111,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UQCRFS1 as ready","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T20:46:37.988796+11:00","panel_name":"Hypertrophic cardiomyopathy_VCGS","panel_id":111,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uqcrfs1 has been classified as Green List (High Evidence).","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T20:46:15.198061+11:00","panel_name":"Hypertrophic cardiomyopathy_VCGS","panel_id":111,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UQCRFS1 as Green List (high evidence)","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T20:46:15.186236+11:00","panel_name":"Hypertrophic cardiomyopathy_VCGS","panel_id":111,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uqcrfs1 has been classified as Green List (High Evidence).","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T20:45:39.243376+11:00","panel_name":"Hypertrophic cardiomyopathy_VCGS","panel_id":111,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UQCRFS1 was added\ngene: UQCRFS1 was added to Hypertrophic cardiomyopathy_VCGS. Sources: Literature\nMode of inheritance for gene: UQCRFS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: UQCRFS1 were set to 31883641\nPhenotypes for gene: UQCRFS1 were set to Mitochondrial Complex III deficiency; lactic acidosis; fetal bradycardia; hypertrophic cardiomyopathy; alopecia totalis\nReview for gene: UQCRFS1 was set to GREEN\nAdded comment: Two unrelated families reported plus functional evidence. \nSources: Literature","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T18:56:40.737505+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.537","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UQCRFS1 as ready","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T18:56:40.725181+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.537","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uqcrfs1 has been classified as Green List (High Evidence).","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T18:56:33.300278+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.537","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UQCRFS1 as Green List (high evidence)","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T18:56:33.289400+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.537","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uqcrfs1 has been classified as Green List (High Evidence).","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T18:56:14.433857+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.536","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UQCRFS1 was added\ngene: UQCRFS1 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: UQCRFS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: UQCRFS1 were set to 31883641\nPhenotypes for gene: UQCRFS1 were set to Mitochondrial Complex III deficiency; lactic acidosis; fetal bradycardia; hypertrophic cardiomyopathy; alopecia totalis\nReview for gene: UQCRFS1 was set to GREEN\nAdded comment: Two unrelated families reported plus functional evidence. \nSources: Literature","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T18:54:04.038858+11:00","panel_name":"Mitochondrial_AustralianGenomics_VCGS","panel_id":203,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UQCRFS1 as ready","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T18:54:04.027695+11:00","panel_name":"Mitochondrial_AustralianGenomics_VCGS","panel_id":203,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uqcrfs1 has been classified as Green List (High Evidence).","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T18:53:56.475920+11:00","panel_name":"Mitochondrial_AustralianGenomics_VCGS","panel_id":203,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UQCRFS1 as Green List (high evidence)","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T18:53:56.464334+11:00","panel_name":"Mitochondrial_AustralianGenomics_VCGS","panel_id":203,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uqcrfs1 has been classified as Green List (High Evidence).","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T18:53:21.001644+11:00","panel_name":"Mitochondrial_AustralianGenomics_VCGS","panel_id":203,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UQCRFS1 was added\ngene: UQCRFS1 was added to Mitochondrial_AustralianGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: UQCRFS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: UQCRFS1 were set to 31883641\nPhenotypes for gene: UQCRFS1 were set to Mitochondrial Complex III deficiency; lactic acidosis; fetal bradycardia; hypertrophic cardiomyopathy; alopecia totalis\nReview for gene: UQCRFS1 was set to GREEN\nAdded comment: Two unrelated families reported plus functional evidence. \nSources: Literature","entity_name":"UQCRFS1","entity_type":"gene"},{"created":"2020-01-02T16:58:19.719193+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.222","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSPEAR as ready","entity_name":"TSPEAR","entity_type":"gene"},{"created":"2020-01-02T16:58:19.707540+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.222","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tspear has been classified as Red List (Low Evidence).","entity_name":"TSPEAR","entity_type":"gene"},{"created":"2020-01-02T16:58:16.340170+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.222","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSPEAR were changed from Deafness, autosomal recessive 98, MIM#614861 to Deafness, autosomal recessive 98, MIM#614861","entity_name":"TSPEAR","entity_type":"gene"},{"created":"2020-01-02T16:57:54.674984+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.221","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSPEAR were changed from  to Deafness, autosomal recessive 98, MIM#614861","entity_name":"TSPEAR","entity_type":"gene"},{"created":"2020-01-02T16:57:31.735457+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.220","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TSPEAR were set to ","entity_name":"TSPEAR","entity_type":"gene"},{"created":"2020-01-02T16:57:07.519550+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.220","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TSPEAR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TSPEAR","entity_type":"gene"},{"created":"2020-01-02T16:56:38.358886+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.219","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TSPEAR as Red List (low evidence)","entity_name":"TSPEAR","entity_type":"gene"},{"created":"2020-01-02T16:56:38.346706+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.219","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tspear has been classified as Red List (Low Evidence).","entity_name":"TSPEAR","entity_type":"gene"},{"created":"2020-01-02T16:56:04.970641+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.218","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TSPEAR: Rating: RED; Mode of pathogenicity: None; Publications: 22678063, 26969326; Phenotypes: Deafness, autosomal recessive 98, MIM#614861; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TSPEAR","entity_type":"gene"},{"created":"2020-01-02T16:49:03.589196+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.218","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TNC as ready","entity_name":"TNC","entity_type":"gene"},{"created":"2020-01-02T16:49:03.578006+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.218","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnc has been classified as Amber List (Moderate Evidence).","entity_name":"TNC","entity_type":"gene"},{"created":"2020-01-02T16:48:56.931458+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.218","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TNC were changed from  to Deafness, autosomal dominant 56, MIM# 615629","entity_name":"TNC","entity_type":"gene"},{"created":"2020-01-02T16:48:33.398951+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.217","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TNC were set to ","entity_name":"TNC","entity_type":"gene"},{"created":"2020-01-02T16:48:00.572252+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.216","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TNC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TNC","entity_type":"gene"},{"created":"2020-01-02T16:47:29.747612+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.215","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TNC as Amber List (moderate evidence)","entity_name":"TNC","entity_type":"gene"},{"created":"2020-01-02T16:47:29.735844+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.215","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnc has been classified as Amber List (Moderate Evidence).","entity_name":"TNC","entity_type":"gene"},{"created":"2020-01-02T16:46:55.285725+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.214","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TNC: Rating: AMBER; Mode of pathogenicity: None; Publications: 23936043; Phenotypes: Deafness, autosomal dominant 56, MIM# 615629; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TNC","entity_type":"gene"},{"created":"2020-01-02T16:42:26.636880+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.214","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TJP2 as ready","entity_name":"TJP2","entity_type":"gene"},{"created":"2020-01-02T16:42:26.624238+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.214","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tjp2 has been classified as Red List (Low Evidence).","entity_name":"TJP2","entity_type":"gene"},{"created":"2020-01-02T16:36:56.342102+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.214","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TJP2 were changed from Deafness to Deafness","entity_name":"TJP2","entity_type":"gene"},{"created":"2020-01-02T16:36:34.499882+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.214","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TJP2 were set to 24752540; 20602916; 18616530","entity_name":"TJP2","entity_type":"gene"},{"created":"2020-01-02T16:35:56.761473+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.213","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TJP2 were changed from  to Deafness","entity_name":"TJP2","entity_type":"gene"},{"created":"2020-01-02T16:35:21.199747+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.213","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TJP2 were set to ","entity_name":"TJP2","entity_type":"gene"},{"created":"2020-01-02T16:34:51.527437+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.213","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TJP2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TJP2","entity_type":"gene"},{"created":"2020-01-02T16:34:14.653136+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.212","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TJP2 as Red List (low evidence)","entity_name":"TJP2","entity_type":"gene"},{"created":"2020-01-02T16:34:14.638943+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.212","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tjp2 has been classified as Red List (Low Evidence).","entity_name":"TJP2","entity_type":"gene"},{"created":"2020-01-02T16:33:40.361263+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TJP2: Rating: RED; Mode of pathogenicity: None; Publications: 24752540, 20602916, 18616530; Phenotypes: Deafness; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TJP2","entity_type":"gene"},{"created":"2020-01-02T16:25:34.181208+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC26A5 as ready","entity_name":"SLC26A5","entity_type":"gene"},{"created":"2020-01-02T16:25:34.175071+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Another publication identified, plus another individual with bi-allelic variants reported by a diagnostic laboratory.","entity_name":"SLC26A5","entity_type":"gene"},{"created":"2020-01-02T16:25:34.143923+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc26a5 has been classified as Green List (High Evidence).","entity_name":"SLC26A5","entity_type":"gene"},{"created":"2020-01-02T16:25:07.577248+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"SLC26A5","entity_type":"gene"},{"created":"2020-01-02T16:25:03.831542+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment on publications: Another another individual with bi-allelic variants reported by a diagnostic laboratory.","entity_name":"SLC26A5","entity_type":"gene"},{"created":"2020-01-02T16:25:03.808420+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.211","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC26A5 were set to 24164807; 26969326","entity_name":"SLC26A5","entity_type":"gene"},{"created":"2020-01-02T16:24:39.941857+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.210","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment on publications: Another another individual with bi-allelic variants reported by a diagnostic laboratory.","entity_name":"SLC26A5","entity_type":"gene"},{"created":"2020-01-02T16:24:39.917853+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.210","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC26A5 were set to 24164807","entity_name":"SLC26A5","entity_type":"gene"},{"created":"2020-01-02T16:23:46.711003+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.209","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC26A5 as Green List (high evidence)","entity_name":"SLC26A5","entity_type":"gene"},{"created":"2020-01-02T16:23:46.691668+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.209","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc26a5 has been classified as Green List (High Evidence).","entity_name":"SLC26A5","entity_type":"gene"},{"created":"2020-01-02T16:05:23.245139+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MPZL2 as ready","entity_name":"MPZL2","entity_type":"gene"},{"created":"2020-01-02T16:05:23.228787+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mpzl2 has been classified as Green List (High Evidence).","entity_name":"MPZL2","entity_type":"gene"},{"created":"2020-01-02T16:05:16.850255+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.208","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MPZL2 were set to ","entity_name":"MPZL2","entity_type":"gene"},{"created":"2020-01-02T16:04:50.687022+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.207","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MPZL2 were changed from  to Deafness, autosomal recessive 111, MIM#618145","entity_name":"MPZL2","entity_type":"gene"},{"created":"2020-01-02T16:04:26.707756+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.206","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MPZL2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MPZL2","entity_type":"gene"},{"created":"2020-01-02T16:03:37.194816+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.205","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MPZL2: Rating: GREEN; Mode of pathogenicity: None; Publications: 29982980, 29961571; Phenotypes: Deafness, autosomal recessive 111, MIM#618145; Mode of inheritance: None","entity_name":"MPZL2","entity_type":"gene"},{"created":"2020-01-02T15:59:39.669327+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.205","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LMX1A as ready","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:59:39.663441+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.205","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Two families with mono-allelic variants and dominant pattern of deafness, one family with bi-allelic variants. Mouse model.","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:59:39.635013+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.205","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lmx1a has been classified as Amber List (Moderate Evidence).","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:59:37.148264+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.205","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LMX1A were changed from  to Deafness, autosomal recessive and autosomal dominant","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:59:13.521819+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.204","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LMX1A were set to ","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:57:48.418522+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.203","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LMX1A was changed from BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:57:21.190933+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.202","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LMX1A as Amber List (moderate evidence)","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:57:21.179921+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.202","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lmx1a has been classified as Amber List (Moderate Evidence).","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:56:58.727261+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.201","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LMX1A was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:56:35.422258+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.201","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LMX1A as Amber List (moderate evidence)","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:56:35.355884+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.201","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lmx1a has been classified as Amber List (Moderate Evidence).","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:54:40.368198+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.200","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LMX1A: Rating: AMBER; Mode of pathogenicity: None; Publications: 29971487; Phenotypes: Deafness, autosomal recessive; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LMX1A","entity_type":"gene"},{"created":"2020-01-02T15:49:48.238748+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.200","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HGF as ready","entity_name":"HGF","entity_type":"gene"},{"created":"2020-01-02T15:49:48.233451+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.200","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Note founder variants are synonymous (S165S) or deep intronic, c.482+1986_1988, c.482+1991_2000del","entity_name":"HGF","entity_type":"gene"},{"created":"2020-01-02T15:49:48.205792+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.200","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hgf has been classified as Green List (High Evidence).","entity_name":"HGF","entity_type":"gene"},{"created":"2020-01-02T15:49:07.420175+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.200","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HGF were set to ","entity_name":"HGF","entity_type":"gene"},{"created":"2020-01-02T15:37:22.881000+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.199","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GJB6 as Red List (low evidence)","entity_name":"GJB6","entity_type":"gene"},{"created":"2020-01-02T15:37:22.862004+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.199","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gjb6 has been classified as Red List (Low Evidence).","entity_name":"GJB6","entity_type":"gene"},{"created":"2020-01-02T15:37:07.786677+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.198","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GJB6 as ready","entity_name":"GJB6","entity_type":"gene"},{"created":"2020-01-02T15:37:07.773506+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.198","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gjb6 has been classified as Red List (Low Evidence).","entity_name":"GJB6","entity_type":"gene"},{"created":"2020-01-02T15:36:58.416984+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.198","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GJB6 were changed from  to Deafness, autosomal recessive and autosomal dominant","entity_name":"GJB6","entity_type":"gene"},{"created":"2020-01-02T15:36:33.982609+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.198","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GJB6 as Red List (low evidence)","entity_name":"GJB6","entity_type":"gene"},{"created":"2020-01-02T15:36:33.918435+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.198","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gjb6 has been classified as Red List (Low Evidence).","entity_name":"GJB6","entity_type":"gene"},{"created":"2020-01-02T15:35:59.924532+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GJB6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Deafness, autosomal recessive and autosomal dominant; Mode of inheritance: None","entity_name":"GJB6","entity_type":"gene"},{"created":"2020-01-02T15:30:18.267561+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GJB4 as ready","entity_name":"GJB4","entity_type":"gene"},{"created":"2020-01-02T15:30:18.256347+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gjb4 has been classified as Red List (Low Evidence).","entity_name":"GJB4","entity_type":"gene"},{"created":"2020-01-02T15:30:14.052628+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GJB4 as Red List (low evidence)","entity_name":"GJB4","entity_type":"gene"},{"created":"2020-01-02T15:30:14.041311+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gjb4 has been classified as Red List (Low Evidence).","entity_name":"GJB4","entity_type":"gene"},{"created":"2020-01-02T15:29:40.533686+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.196","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GJB4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: Unknown","entity_name":"GJB4","entity_type":"gene"},{"created":"2020-01-02T15:23:34.511870+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.196","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GJB1 as ready","entity_name":"GJB1","entity_type":"gene"}]}