{"count":220725,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1563","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1561","results":[{"created":"2020-10-01T13:49:42.295553+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.533","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pax3 has been classified as Green List (High Evidence).","entity_name":"PAX3","entity_type":"gene"},{"created":"2020-10-01T13:49:31.244921+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.533","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PAX3 were changed from  to Waardenburg syndrome, type 1, MIM# 193500","entity_name":"PAX3","entity_type":"gene"},{"created":"2020-10-01T13:49:04.521151+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.532","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PAX3 were set to ","entity_name":"PAX3","entity_type":"gene"},{"created":"2020-10-01T13:48:29.446517+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.531","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PAX3 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"PAX3","entity_type":"gene"},{"created":"2020-10-01T13:48:05.416577+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.530","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PAX3: Rating: GREEN; Mode of pathogenicity: None; Publications: 27759048, 7897628, 28690861, 30314436, 25932447, 7726174, 12949970; Phenotypes: Waardenburg syndrome, type 1, MIM# 193500; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"PAX3","entity_type":"gene"},{"created":"2020-10-01T11:58:43.301390+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4714","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OTOGL as ready","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:58:43.252213+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4714","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: otogl has been classified as Green List (High Evidence).","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:58:36.596289+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4714","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OTOGL were changed from  to Deafness, autosomal recessive 84B, MIM# 614944","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:57:26.965717+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4713","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OTOGL were set to ","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:57:07.852386+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4712","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OTOGL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:56:49.708377+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4711","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: OTOGL: Rating: GREEN; Mode of pathogenicity: None; Publications: 23122586, 23850727, 25829320, ​25719458, 28426234; Phenotypes: Deafness, autosomal recessive 84B, MIM# 614944; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:55:59.902269+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.530","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OTOGL as ready","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:55:59.887240+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.530","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: otogl has been classified as Green List (High Evidence).","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:55:56.881563+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.530","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OTOGL were changed from Deafness, autosomal recessive 84B, MIM# 614944 to Deafness, autosomal recessive 84B, MIM# 614944","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:55:42.855813+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.530","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OTOGL were changed from  to Deafness, autosomal recessive 84B, MIM# 614944","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:55:21.796025+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.529","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OTOGL were set to ","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:54:56.720454+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.528","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OTOGL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:54:29.815833+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.527","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: OTOGL: Rating: GREEN; Mode of pathogenicity: None; Publications: 23122586, 23850727, 25829320, ​25719458, 28426234; Phenotypes: Deafness, autosomal recessive 84B, MIM# 614944; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"OTOGL","entity_type":"gene"},{"created":"2020-10-01T11:51:55.146676+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RDX as ready","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:51:55.135411+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rdx has been classified as Green List (High Evidence).","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:51:51.842863+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RDX were changed from Deafness, autosomal recessive to Deafness, autosomal recessive 24, MIM# 611022","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:51:29.009904+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RDX were set to ","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:51:15.760388+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RDX as Green List (high evidence)","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:51:15.751974+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rdx has been classified as Green List (High Evidence).","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:51:03.508772+10:00","panel_name":"Newborn Screening_BabySeq","panel_id":3302,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RDX: Rating: GREEN; Mode of pathogenicity: None; Publications: 17226784, 19215054, 22567349, 26226137, 15314067; Phenotypes: Deafness, autosomal recessive 24, MIM# 611022; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:49:30.858235+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4711","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RDX as ready","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:49:30.844687+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4711","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rdx has been classified as Green List (High Evidence).","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:49:24.364370+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4711","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RDX were changed from  to Deafness, autosomal recessive 24, MIM# 611022","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:49:06.289381+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4710","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RDX were set to ","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:48:46.134563+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4709","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RDX was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:48:00.697891+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4708","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RDX: Rating: GREEN; Mode of pathogenicity: None; Publications: 17226784, 19215054, 22567349, 26226137, 15314067; Phenotypes: Deafness, autosomal recessive 24, MIM# 611022; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:47:17.511812+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.527","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RDX as ready","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:47:17.498168+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.527","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rdx has been classified as Green List (High Evidence).","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:46:46.665078+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.527","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RDX were changed from  to Deafness, autosomal recessive 24, MIM# 611022","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:46:23.603058+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.526","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RDX were set to ","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:45:56.037243+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.525","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RDX was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:45:31.846193+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.524","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RDX: Rating: GREEN; Mode of pathogenicity: None; Publications: 17226784, 19215054, 22567349, 26226137, 15314067; Phenotypes: Deafness, autosomal recessive 24, MIM# 611022; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RDX","entity_type":"gene"},{"created":"2020-10-01T11:32:17.205602+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3038","user_name":"Ee Ming Wong","item_type":"entity","text":"reviewed gene: ARID2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 26238514; Phenotypes: neurodevelopmental delay, global developmental delay, gross motor delay; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes","entity_name":"ARID2","entity_type":"gene"},{"created":"2020-10-01T11:20:47.447555+10:00","panel_name":"Progressive Neurological Conditions","panel_id":3377,"panel_version":"0.1","user_name":"Bryony Thompson","item_type":"panel","text":"Changed child panels to: Myopathy - paediatric onset; Ataxia - paediatric; Leukodystrophy - paediatric; Hereditary Spastic Paraplegia - paediatric; Dystonia - complex; Ataxia - adult onset; Early-onset Dementia; Motor Neuron Disease; Myopathy - adult onset; Early-onset Parkinson disease; Hereditary Neuropathy - complex; Leukodystrophy - adult onset; Limb Girdle Muscular Dystrophy; Hereditary Neuropathy_CMT - isolated; Brain Calcification; Hereditary Spastic Paraplegia - adult onset; Brain Channelopathies; Dystonia - isolated/combined","entity_name":null,"entity_type":null},{"created":"2020-10-01T11:07:30.908445+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4708","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OTOA as ready","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T11:07:30.899314+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4708","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: otoa has been classified as Green List (High Evidence).","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T11:07:23.534015+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4708","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OTOA were changed from  to Deafness, autosomal recessive 22, MIM# 607039","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T11:07:05.069214+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4707","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OTOA were set to ","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T11:06:27.125026+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4706","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OTOA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T11:06:11.133441+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4705","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: OTOA: Rating: GREEN; Mode of pathogenicity: None; Publications: 11972037, 19888295, 23173898, 16460646, 26029705, 26969326, 23129639; Phenotypes: Deafness, autosomal recessive 22, MIM# 607039; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T11:05:17.967629+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.524","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OTOA as ready","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T11:05:17.959047+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.524","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: otoa has been classified as Green List (High Evidence).","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T11:05:15.775873+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.524","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OTOA were changed from  to Deafness, autosomal recessive 22, MIM# 607039","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T11:04:47.812092+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.523","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OTOA were set to ","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T11:04:23.821517+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.522","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OTOA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T11:03:56.550102+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.521","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: OTOA: Rating: GREEN; Mode of pathogenicity: None; Publications: 11972037, 19888295, 23173898, 16460646, 26029705, 26969326, 23129639; Phenotypes: Deafness, autosomal recessive 22, MIM# 607039; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"OTOA","entity_type":"gene"},{"created":"2020-10-01T10:59:13.275551+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO7A as ready","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:59:13.267212+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo7a has been classified as Green List (High Evidence).","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:59:09.745764+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYO7A were set to ","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:58:35.855981+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYO7A: Rating: GREEN; Mode of pathogenicity: None; Publications: 23559863, 18181211, 25211151, 11391666; Phenotypes: Usher syndrome, type 1B, MIM# 276900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:56:26.150528+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4705","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO7A as ready","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:56:26.127354+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4705","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo7a has been classified as Green List (High Evidence).","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:56:08.822244+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4705","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYO7A were changed from  to Deafness, autosomal dominant 11, MIM# 601317; Deafness, autosomal recessive 2, 600060; Usher syndrome, type 1B, MIM# 276900","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:55:49.646562+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4704","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYO7A were set to ","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:55:32.092780+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4703","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYO7A was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:55:14.573121+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4702","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYO7A: Rating: GREEN; Mode of pathogenicity: None; Publications: 9354784, 15300860, 15121790, 15221449, 16449806, 21150918, 23451214, 23383098, 28802369, 29400105, 23559863, 18181211, 25211151; Phenotypes: Deafness, autosomal dominant 11, MIM# 601317, Deafness, autosomal recessive 2, 600060, Usher syndrome, type 1B, MIM# 276900; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:53:58.152687+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.521","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO7A as ready","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:53:58.142334+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.521","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo7a has been classified as Green List (High Evidence).","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:53:33.689897+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.521","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYO7A were changed from  to Deafness, autosomal dominant 11, MIM# 601317; Deafness, autosomal recessive 2, 600060; Usher syndrome, type 1B, MIM# 276900","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:52:59.019089+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.520","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYO7A were set to ","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:52:31.704703+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.519","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYO7A was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:51:59.843468+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.518","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYO7A: Rating: GREEN; Mode of pathogenicity: None; Publications: 9354784, 15300860, 15121790, 15221449, 16449806, 21150918, 23451214, 23383098, 28802369, 29400105, 23559863, 18181211, 25211151; Phenotypes: Deafness, autosomal dominant 11, MIM# 601317, Deafness, autosomal recessive 2, 600060, Usher syndrome, type 1B, MIM# 276900; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MYO7A","entity_type":"gene"},{"created":"2020-10-01T10:33:27.126370+10:00","panel_name":"Progressive Neurological Conditions","panel_id":3377,"panel_version":"0.0","user_name":"Bryony Thompson","item_type":"panel","text":"Added Panel Progressive Neurological Conditions\nSet child panels to: Myopathy - paediatric onset; Ataxia - paediatric; Leukodystrophy - paediatric; Hereditary Spastic Paraplegia - paediatric; Dystonia - complex; Ataxia - adult onset; Early-onset Dementia; Motor Neuron Disease; Myopathy - adult onset; Early-onset Parkinson disease; Hereditary Neuropathy - complex; Leukodystrophy - adult onset; Limb Girdle Muscular Dystrophy; Hereditary Neuropathy_CMT - isolated; Hereditary Spastic Paraplegia - adult onset; Dystonia - isolated/combined\nSet panel types to: Royal Melbourne Hospital; Rare Disease","entity_name":null,"entity_type":null},{"created":"2020-10-01T10:27:54.389850+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.518","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMPX as ready","entity_name":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:27:54.379050+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.518","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smpx has been classified as Green List (High Evidence).","entity_name":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:27:36.970866+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4702","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMPX as ready","entity_name":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:27:36.956658+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4702","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smpx has been classified as Green List (High Evidence).","entity_name":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:23:50.126698+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4702","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMPX were changed from  to Deafness, X-linked 4, MIM# 300066","entity_name":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:23:31.384551+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4701","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMPX were set to ","entity_name":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:23:12.915701+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4700","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMPX 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":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:22:57.411330+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4699","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMPX: Rating: GREEN; Mode of pathogenicity: None; Publications: 21549342, 21549336, 21893181, 22911656, 28542515; Phenotypes: Deafness, X-linked 4, MIM# 300066; 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":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:07:07.936995+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.518","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMPX were changed from Deafness, X-linked 4, MIM# 300066 to Deafness, X-linked 4, MIM# 300066","entity_name":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:06:31.110794+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.517","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMPX were changed from  to Deafness, X-linked 4, MIM# 300066","entity_name":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:05:53.187692+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.516","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMPX were set to ","entity_name":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:05:25.497415+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.515","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMPX 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":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:04:58.223920+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.514","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMPX: Rating: GREEN; Mode of pathogenicity: None; Publications: 21549342, 21549336, 21893181, 22911656, 28542515; Phenotypes: Deafness, X-linked 4, MIM# 300066; 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":"SMPX","entity_type":"gene"},{"created":"2020-10-01T10:01:30.800525+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4699","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO6 as ready","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T10:01:30.790297+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4699","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo6 has been classified as Green List (High Evidence).","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T10:01:23.660185+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4699","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYO6 were changed from  to Deafness, autosomal dominant 22, MIM# 606346; Deafness, autosomal recessive 37, MIM# 607821","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T10:01:05.621751+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4698","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYO6 were set to ","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T10:00:47.309163+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4697","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYO6 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T10:00:29.216693+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4696","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYO6: Rating: GREEN; Mode of pathogenicity: None; Publications: 24105371, 11468689, 25999546, 25227905, 18348273, 27171474; Phenotypes: Deafness, autosomal dominant 22, MIM# 606346, Deafness, autosomal recessive 37, MIM# 607821; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T09:59:41.645743+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.514","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO6 as ready","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T09:59:41.636733+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.514","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo6 has been classified as Green List (High Evidence).","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T09:59:03.420809+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.514","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYO6 were changed from  to Deafness, autosomal dominant 22, MIM# 606346; Deafness, autosomal recessive 37, MIM# 607821","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T09:58:23.541666+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.513","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYO6 were set to ","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T09:57:47.865355+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.512","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYO6 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T09:57:24.199334+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.511","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYO6: Rating: GREEN; Mode of pathogenicity: None; Publications: 24105371, 11468689, 25999546, 25227905, 18348273, 27171474; Phenotypes: Deafness, autosomal dominant 22, MIM# 606346, Deafness, autosomal recessive 37, MIM# 607821; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"MYO6","entity_type":"gene"},{"created":"2020-10-01T09:51:25.768882+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4696","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO15A as ready","entity_name":"MYO15A","entity_type":"gene"},{"created":"2020-10-01T09:51:25.756187+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4696","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo15a has been classified as Green List (High Evidence).","entity_name":"MYO15A","entity_type":"gene"},{"created":"2020-10-01T09:51:17.355031+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4696","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYO15A were changed from  to Deafness, autosomal recessive 3, MIM# 600316","entity_name":"MYO15A","entity_type":"gene"},{"created":"2020-10-01T09:50:54.342185+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4695","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYO15A were set to ","entity_name":"MYO15A","entity_type":"gene"},{"created":"2020-10-01T09:50:36.026216+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4694","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYO15A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYO15A","entity_type":"gene"},{"created":"2020-10-01T09:50:11.376050+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4693","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYO15A: Rating: GREEN; Mode of pathogenicity: None; Publications: 27375115, 26226137, 23208854, 19309289, 9603735, 10915760; Phenotypes: Deafness, autosomal recessive 3, MIM# 600316; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYO15A","entity_type":"gene"},{"created":"2020-10-01T09:49:15.771810+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.511","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO15A as ready","entity_name":"MYO15A","entity_type":"gene"}]}