{"count":220725,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2019","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2017","results":[{"created":"2019-12-31T13:25:01.561794+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lars2 has been classified as Green List (High Evidence).","entity_name":"LARS2","entity_type":"gene"},{"created":"2019-12-31T13:24:58.938132+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LARS2 were changed from  to Perrault syndrome 4, MIM#615300","entity_name":"LARS2","entity_type":"gene"},{"created":"2019-12-31T13:24:05.393183+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARS2","entity_type":"gene"},{"created":"2019-12-31T13:22:56.077333+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.473","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KITLG as ready","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T13:22:56.061397+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.473","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kitlg has been classified as Amber List (Moderate Evidence).","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T13:22:47.897453+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.473","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KITLG was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T13:22:21.371802+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.472","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KITLG were set to ","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T13:15:24.338770+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.471","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KITLG were changed from  to Deafness, autosomal dominant 69, unilateral or asymmetric, MIM# 616697","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T13:14:58.249885+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.470","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KITLG as Amber List (moderate evidence)","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T13:14:58.237080+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.470","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kitlg has been classified as Amber List (Moderate Evidence).","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T13:14:40.646014+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.469","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KITLG: Rating: AMBER; Mode of pathogenicity: None; Publications: 26522471; Phenotypes: Deafness, autosomal dominant 69, unilateral or asymmetric, MIM# 616697; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T13:12:40.308011+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MCM2 as ready","entity_name":"MCM2","entity_type":"gene"},{"created":"2019-12-31T13:12:40.296451+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcm2 has been classified as Red List (Low Evidence).","entity_name":"MCM2","entity_type":"gene"},{"created":"2019-12-31T13:12:36.499882+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MCM2 as Red List (low evidence)","entity_name":"MCM2","entity_type":"gene"},{"created":"2019-12-31T13:12:36.484862+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcm2 has been classified as Red List (Low Evidence).","entity_name":"MCM2","entity_type":"gene"},{"created":"2019-12-31T13:11:26.260021+11:00","panel_name":"Autism_VCGS","panel_id":51,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MET as ready","entity_name":"MET","entity_type":"gene"},{"created":"2019-12-31T13:11:26.247897+11:00","panel_name":"Autism_VCGS","panel_id":51,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: met has been classified as Red List (Low Evidence).","entity_name":"MET","entity_type":"gene"},{"created":"2019-12-31T13:11:03.001122+11:00","panel_name":"Autism_VCGS","panel_id":51,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MET were changed from  to ?Deafness, autosomal recessive 97, OMIM #616705; {Osteofibrous dysplasia, susceptibility to}, OMIM #607278","entity_name":"MET","entity_type":"gene"},{"created":"2019-12-31T13:10:40.154298+11:00","panel_name":"Autism_VCGS","panel_id":51,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MET was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MET","entity_type":"gene"},{"created":"2019-12-31T13:10:18.512442+11:00","panel_name":"Autism_VCGS","panel_id":51,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MET as Red List (low evidence)","entity_name":"MET","entity_type":"gene"},{"created":"2019-12-31T13:10:18.447657+11:00","panel_name":"Autism_VCGS","panel_id":51,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: met has been classified as Red List (Low Evidence).","entity_name":"MET","entity_type":"gene"},{"created":"2019-12-31T13:07:24.305694+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIR96 as ready","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:07:24.294719+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir96 has been classified as Amber List (Moderate Evidence).","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:07:11.794035+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MIR96 were changed from Autosomal dominant hearing loss to Deafness, autosomal dominant 50, MIM# 613074","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:06:36.328943+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.469","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MIR96 were changed from  to Deafness, autosomal dominant 50, MIM# 613074","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:06:23.719795+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.468","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MIR96 were set to ","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:06:10.498500+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.467","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MIR96 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:05:53.670553+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.466","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MIR96 as Amber List (moderate evidence)","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:05:53.658393+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.466","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir96 has been classified as Amber List (Moderate Evidence).","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:05:35.735588+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.465","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MIR96: Rating: AMBER; Mode of pathogenicity: None; Publications: 19363479, 29325119; Phenotypes: Deafness, autosomal dominant 50, MIM# 613074; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:03:36.531839+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIR96 as ready","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:03:36.519833+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir96 has been classified as Amber List (Moderate Evidence).","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:02:44.694914+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MIR96 were changed from  to Autosomal dominant hearing loss","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:02:02.701198+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MIR96 were set to ","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T13:01:42.438572+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MIR96 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T12:59:29.709248+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MIR96 as Amber List (moderate evidence)","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T12:59:29.696971+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir96 has been classified as Amber List (Moderate Evidence).","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T12:50:25.322592+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYO3A: Rating: GREEN; Mode of pathogenicity: None; Publications: 21165622, 26754646, 23990876; Phenotypes: Deafness, autosomal recessive 30, MIM# 607101; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYO3A","entity_type":"gene"},{"created":"2019-12-31T12:46:57.678091+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYH14 as ready","entity_name":"MYH14","entity_type":"gene"},{"created":"2019-12-31T12:46:57.667064+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myh14 has been classified as Green List (High Evidence).","entity_name":"MYH14","entity_type":"gene"},{"created":"2019-12-31T12:46:52.490766+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYH14 were changed from Deafness, autosomal dominant 4A, MIM# 600652 to Deafness, autosomal dominant 4A, MIM# 600652","entity_name":"MYH14","entity_type":"gene"},{"created":"2019-12-31T12:46:32.422628+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYH14 were changed from  to Deafness, autosomal dominant 4A, MIM# 600652","entity_name":"MYH14","entity_type":"gene"},{"created":"2019-12-31T12:46:11.621620+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYH14 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYH14","entity_type":"gene"},{"created":"2019-12-31T12:45:36.437308+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYH14: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Deafness, autosomal dominant 4A, MIM# 600652; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYH14","entity_type":"gene"},{"created":"2019-12-31T12:45:07.390237+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.81","user_name":"Lilian Rudd","item_type":"entity","text":"reviewed gene: MIR96: Rating: AMBER; Mode of pathogenicity: None; Publications: 19363479, 29325119; Phenotypes: Autosomal dominant hearing loss; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MIR96","entity_type":"gene"},{"created":"2019-12-31T12:44:04.114060+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MSRB3 as ready","entity_name":"MSRB3","entity_type":"gene"},{"created":"2019-12-31T12:44:04.103044+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: msrb3 has been classified as Green List (High Evidence).","entity_name":"MSRB3","entity_type":"gene"},{"created":"2019-12-31T12:44:00.534077+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MSRB3 were changed from  to Deafness, autosomal recessive 74, MIM# 613718","entity_name":"MSRB3","entity_type":"gene"},{"created":"2019-12-31T12:43:37.786268+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MSRB3 were set to ","entity_name":"MSRB3","entity_type":"gene"},{"created":"2019-12-31T12:43:02.279216+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MSRB3: Rating: ; Mode of pathogenicity: None; Publications: 19650862, 24191262, 21185009; Phenotypes: Deafness, autosomal recessive 74, MIM# 613718; Mode of inheritance: None","entity_name":"MSRB3","entity_type":"gene"},{"created":"2019-12-31T12:39:50.291918+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MET as ready","entity_name":"MET","entity_type":"gene"},{"created":"2019-12-31T12:39:50.278355+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: met has been classified as Red List (Low Evidence).","entity_name":"MET","entity_type":"gene"},{"created":"2019-12-31T12:39:24.090419+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MET was added\ngene: MET was added to Deafness_MelbourneGenomics_VCGS. Sources: Expert list\nMode of inheritance for gene: MET was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MET were set to 25941349; 31801140\nPhenotypes for gene: MET were set to Deafness, autosomal recessive 97, MIM#\t616705\nReview for gene: MET was set to RED\nAdded comment: Two families reported, no functional data. \nSources: Expert list","entity_name":"MET","entity_type":"gene"},{"created":"2019-12-31T12:37:51.836501+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.78","user_name":"Lilian Rudd","item_type":"entity","text":"gene: MCM2 was added\ngene: MCM2 was added to Deafness_MelbourneGenomics_VCGS. Sources: Expert list\nMode of inheritance for gene: MCM2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: MCM2 were set to 26196677\nPhenotypes for gene: MCM2 were set to Autosomal dominant hearing loss\nReview for gene: MCM2 was set to RED\nAdded comment: One family, expression studies. \nSources: Expert list","entity_name":"MCM2","entity_type":"gene"},{"created":"2019-12-31T12:34:22.753598+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KITLG as ready","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T12:34:22.741501+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kitlg has been classified as Amber List (Moderate Evidence).","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T12:34:18.866060+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KITLG as Amber List (moderate evidence)","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T12:34:18.854312+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kitlg has been classified as Amber List (Moderate Evidence).","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T12:34:10.558331+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.77","user_name":"Lilian Rudd","item_type":"entity","text":"reviewed gene: LARS2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23541342, 27650058, 26970254, 26657938, 28832386, 28000701, 29205794; Phenotypes: Perrault syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARS2","entity_type":"gene"},{"created":"2019-12-31T12:33:49.006086+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KITLG was added\ngene: KITLG was added to Deafness_MelbourneGenomics_VCGS. Sources: Expert list\nMode of inheritance for gene: KITLG was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: KITLG were set to 26522471\nPhenotypes for gene: KITLG were set to Deafness, autosomal dominant 69, unilateral or asymmetric, MIM#\t616697\nReview for gene: KITLG was set to AMBER\nAdded comment: Two unrelated families, limited functional data. \nSources: Expert list","entity_name":"KITLG","entity_type":"gene"},{"created":"2019-12-31T12:30:40.674580+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.76","user_name":"Lilian Rudd","item_type":"entity","text":"reviewed gene: KCNJ10: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"KCNJ10","entity_type":"gene"},{"created":"2019-12-31T12:29:20.212902+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KCNE1 as ready","entity_name":"KCNE1","entity_type":"gene"},{"created":"2019-12-31T12:29:20.200393+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcne1 has been classified as Green List (High Evidence).","entity_name":"KCNE1","entity_type":"gene"},{"created":"2019-12-31T12:29:16.355329+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KCNE1 were changed from Jervell and Lange-Nielsen syndrome 2, MIM# 612347 to Jervell and Lange-Nielsen syndrome 2, MIM# 612347","entity_name":"KCNE1","entity_type":"gene"},{"created":"2019-12-31T12:28:54.746210+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KCNE1 were changed from  to Jervell and Lange-Nielsen syndrome 2, MIM# 612347","entity_name":"KCNE1","entity_type":"gene"},{"created":"2019-12-31T12:28:31.252677+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KCNE1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KCNE1","entity_type":"gene"},{"created":"2019-12-31T12:27:44.190083+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KCNE1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Jervell and Lange-Nielsen syndrome 2, MIM# 612347; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KCNE1","entity_type":"gene"},{"created":"2019-12-31T12:26:43.800134+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.74","user_name":"Lilian Rudd","item_type":"entity","text":"reviewed gene: KARS: Rating: GREEN; Mode of pathogenicity: None; Publications: 23768514, 23768514, 14975237; Phenotypes: autosomal recessive sensorineural hearing loss; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KARS","entity_type":"gene"},{"created":"2019-12-31T12:26:00.904620+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HOMER2 as ready","entity_name":"HOMER2","entity_type":"gene"},{"created":"2019-12-31T12:26:00.893130+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: homer2 has been classified as Green List (High Evidence).","entity_name":"HOMER2","entity_type":"gene"},{"created":"2019-12-31T12:25:56.998787+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HOMER2 were changed from  to Deafness, autosomal dominant 68, MIM# 616707","entity_name":"HOMER2","entity_type":"gene"},{"created":"2019-12-31T12:25:34.166883+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HOMER2 were set to ","entity_name":"HOMER2","entity_type":"gene"},{"created":"2019-12-31T12:24:58.024081+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HOMER2: Rating: ; Mode of pathogenicity: None; Publications: 25816005, 30047143, 25816005; Phenotypes: Deafness, autosomal dominant 68, MIM# 616707; Mode of inheritance: None","entity_name":"HOMER2","entity_type":"gene"},{"created":"2019-12-31T12:21:40.415992+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.72","user_name":"Lilian Rudd","item_type":"entity","text":"reviewed gene: HARS2: Rating: GREEN; Mode of pathogenicity: None; Publications: 21464306, 27650058, 31827252, 31486067; Phenotypes: Perrault syndrome, autosomal recessive sensorineural hearing loss; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HARS2","entity_type":"gene"},{"created":"2019-12-31T12:21:11.348480+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HGF as ready","entity_name":"HGF","entity_type":"gene"},{"created":"2019-12-31T12:21:11.335988+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.72","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":"2019-12-31T12:21:08.604237+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HGF were changed from  to Deafness, autosomal recessive 39, MIM# 608265","entity_name":"HGF","entity_type":"gene"},{"created":"2019-12-31T12:20:36.330299+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HGF: Rating: GREEN; Mode of pathogenicity: None; Publications: 19576567; Phenotypes: Deafness, autosomal recessive 39, MIM# 608265; Mode of inheritance: None","entity_name":"HGF","entity_type":"gene"},{"created":"2019-12-31T12:17:11.386755+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HARS were set to 22279524","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T12:17:03.775139+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HARS as ready","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T12:17:03.762393+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hars has been classified as Red List (Low Evidence).","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T12:16:25.925973+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HARS were changed from Usher syndrome type 3B, MIM# 614504 to Usher syndrome type 3B, MIM# 614504","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T12:16:05.395111+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HARS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T12:15:44.999219+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HARS were changed from  to Usher syndrome type 3B, MIM# 614504","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T12:15:25.888833+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.68","user_name":"Lilian Rudd","item_type":"entity","text":"changed review comment from: Single family with multiple sibs, function studies.; to: Single family with multiple sibs, function studies. 'Moderate' classification from ClinGen expert panel.","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T12:15:21.902488+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HARS were set to ","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T12:14:57.844010+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HARS as Red List (low evidence)","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T12:14:57.799362+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hars has been classified as Red List (Low Evidence).","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T12:14:36.948888+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.67","user_name":"Lilian Rudd","item_type":"entity","text":"reviewed gene: GRXCR2: Rating: AMBER; Mode of pathogenicity: None; Publications: 24619944; Phenotypes: autosomal recessive sensorineural hearing loss; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T12:14:25.570272+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HARS: Rating: RED; Mode of pathogenicity: None; Publications: 22279524; Phenotypes: Usher syndrome type 3B, MIM# 614504; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T12:10:11.104461+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GRHL2 as ready","entity_name":"GRHL2","entity_type":"gene"},{"created":"2019-12-31T12:10:11.093387+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: grhl2 has been classified as Green List (High Evidence).","entity_name":"GRHL2","entity_type":"gene"},{"created":"2019-12-31T12:10:08.420746+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GRHL2 were changed from Deafness, autosomal dominant 28, MIM# 608641 to Deafness, autosomal dominant 28, MIM# 608641","entity_name":"GRHL2","entity_type":"gene"},{"created":"2019-12-31T12:09:44.694365+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GRHL2 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GRHL2","entity_type":"gene"},{"created":"2019-12-31T12:09:08.211408+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.65","user_name":"Lilian Rudd","item_type":"entity","text":"reviewed gene: FOXI1: Rating: GREEN; Mode of pathogenicity: None; Publications: 29242249, 9843211; Phenotypes: sensorineural deafness and distal renal tubular acidosis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FOXI1","entity_type":"gene"},{"created":"2019-12-31T12:09:05.360186+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GRHL2 were changed from  to Deafness, autosomal dominant 28, MIM# 608641","entity_name":"GRHL2","entity_type":"gene"},{"created":"2019-12-31T12:08:42.483347+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GRHL2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GRHL2","entity_type":"gene"},{"created":"2019-12-31T12:08:11.899718+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GRHL2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Deafness, autosomal dominant 28, MIM# 608641; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GRHL2","entity_type":"gene"},{"created":"2019-12-31T12:06:26.355131+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GJB3 were changed from Deafness, autosomal dominant 2B, MIM# 612644 to Deafness, autosomal dominant 2B, MIM# 612644","entity_name":"GJB3","entity_type":"gene"},{"created":"2019-12-31T12:06:10.668036+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GJB3 as ready","entity_name":"GJB3","entity_type":"gene"}]}