{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1917","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1915","results":[{"created":"2020-02-29T20:42:00.429656+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBC1D7 were changed from  to Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:41:33.551962+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBC1D7 were set to ","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:41:09.770908+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBC1D7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:40:42.159387+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TBC1D7 as Amber List (moderate evidence)","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:40:42.150432+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbc1d7 has been classified as Amber List (Moderate Evidence).","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:40:12.576747+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TBC1D7: Rating: AMBER; Mode of pathogenicity: None; Publications: 24515783, 23687350; Phenotypes: Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:39:23.218889+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2285","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBC1D7 as ready","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:39:23.209314+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2285","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbc1d7 has been classified as Amber List (Moderate Evidence).","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:39:14.245931+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2285","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBC1D7 were changed from  to Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:38:42.449940+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2284","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBC1D7 were set to ","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:38:05.837079+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2283","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBC1D7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:37:33.344325+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2282","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TBC1D7 as Amber List (moderate evidence)","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:37:33.335374+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2282","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbc1d7 has been classified as Amber List (Moderate Evidence).","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:37:00.481642+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2281","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TBC1D7: Rating: AMBER; Mode of pathogenicity: None; Publications: 24515783, 23687350; Phenotypes: Macrocephaly/megalencephaly syndrome, autosomal recessive, MIM# 248000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TBC1D7","entity_type":"gene"},{"created":"2020-02-29T20:31:50.981363+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2281","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Four unrelated families reported; two with founder mutation. Protein interacts with KMT2A and KMT2D. Another infant with a de novo missense variant reported in a single infant with multiple congenital abnormalities, insufficient evidence for mono allelic disease at present. \nSources: Literature; to: Four unrelated families reported; two with founder mutation. Protein interacts with KMT2A and KMT2D. Another  de novo missense variant reported in a single infant with multiple congenital abnormalities, insufficient evidence for mono allelic disease at present. \r\nSources: Literature","entity_name":"TASP1","entity_type":"gene"},{"created":"2020-02-29T18:31:07.992529+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAF2 as ready","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:31:07.978830+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taf2 has been classified as Amber List (Moderate Evidence).","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:31:04.367568+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAF2 were changed from  to Mental retardation, autosomal recessive 40, MIM# 615599","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:30:41.880822+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TAF2 were set to ","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:30:14.656191+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:29:52.730266+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAF2 as Amber List (moderate evidence)","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:29:52.721213+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taf2 has been classified as Amber List (Moderate Evidence).","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:29:22.992439+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAF2: Rating: AMBER; Mode of pathogenicity: None; Publications: 21937992, 22633631, 26350204; Phenotypes: Mental retardation, autosomal recessive 40, MIM# 615599; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:28:30.923274+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1533","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAF2 as ready","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:28:30.914492+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1533","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taf2 has been classified as Amber List (Moderate Evidence).","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:28:19.365572+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1533","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAF2 were changed from  to Mental retardation, autosomal recessive 40, MIM# 615599","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:28:02.826989+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1532","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TAF2 were set to ","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:27:45.870121+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1531","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:27:25.036740+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1530","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAF2 as Amber List (moderate evidence)","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:27:25.023701+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1530","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taf2 has been classified as Amber List (Moderate Evidence).","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:27:05.479502+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1529","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAF2: Rating: AMBER; Mode of pathogenicity: None; Publications: 21937992, 22633631, 26350204; Phenotypes: Mental retardation, autosomal recessive 40, MIM# 615599; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:26:45.163440+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2281","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAF2 as ready","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:26:45.154770+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2281","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taf2 has been classified as Amber List (Moderate Evidence).","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:25:55.611354+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2281","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAF2 were changed from  to Mental retardation, autosomal recessive 40, MIM# 615599","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:25:27.254299+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2280","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TAF2 were set to ","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:24:58.627308+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2279","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:24:29.204257+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2278","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAF2 as Amber List (moderate evidence)","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:24:29.190285+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2278","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taf2 has been classified as Amber List (Moderate Evidence).","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:23:57.372044+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2277","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAF2: Rating: AMBER; Mode of pathogenicity: None; Publications: 21937992, 22633631, 26350204; Phenotypes: Mental retardation, autosomal recessive 40, MIM# 615599; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAF2","entity_type":"gene"},{"created":"2020-02-29T18:20:19.421511+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1529","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAF13 as ready","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:20:19.413095+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1529","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taf13 has been classified as Amber List (Moderate Evidence).","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:19:36.100898+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1529","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAF13 were changed from  to Mental retardation, autosomal recessive 60, MIM# 617432","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:19:20.789917+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1528","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TAF13 were set to ","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:18:48.658126+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1527","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAF13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:18:48.110780+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2277","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAF13 as ready","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:18:48.094985+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2277","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taf13 has been classified as Amber List (Moderate Evidence).","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:18:34.498279+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2277","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TAF13 were set to ","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:18:06.586419+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2276","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAF13 were changed from  to Mental retardation, autosomal recessive 60, MIM# 617432","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:17:40.757022+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1526","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAF13 as Amber List (moderate evidence)","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:17:40.748435+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1526","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taf13 has been classified as Amber List (Moderate Evidence).","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:17:20.491054+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1525","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAF13: Rating: AMBER; Mode of pathogenicity: None; Publications: 28257693; Phenotypes: Mental retardation, autosomal recessive 60, MIM# 617432; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:17:16.873451+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2275","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAF13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:16:11.978715+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2274","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAF13 as Amber List (moderate evidence)","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:16:11.965842+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2274","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taf13 has been classified as Amber List (Moderate Evidence).","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:15:38.624561+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2273","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAF13: Rating: AMBER; Mode of pathogenicity: None; Publications: 28257693; Phenotypes: Mental retardation, autosomal recessive 60, MIM# 617432; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAF13","entity_type":"gene"},{"created":"2020-02-29T18:13:33.002871+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TACO1 as ready","entity_name":"TACO1","entity_type":"gene"},{"created":"2020-02-29T18:13:32.992720+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taco1 has been classified as Green List (High Evidence).","entity_name":"TACO1","entity_type":"gene"},{"created":"2020-02-29T18:13:29.752823+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TACO1 were changed from  to Mitochondrial complex IV deficiency; OMIM #220110","entity_name":"TACO1","entity_type":"gene"},{"created":"2020-02-29T18:13:06.943373+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TACO1 were set to ","entity_name":"TACO1","entity_type":"gene"},{"created":"2020-02-29T18:12:37.689259+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TACO1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TACO1","entity_type":"gene"},{"created":"2020-02-29T18:12:08.752900+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TACO1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19503089, 20727754, 25044680, 27319982; Phenotypes: Mitochondrial complex IV deficiency, OMIM #220110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TACO1","entity_type":"gene"},{"created":"2020-02-29T17:34:20.961925+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SYT14 as ready","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:34:20.952261+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: syt14 has been classified as Red List (Low Evidence).","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:34:16.561043+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SYT14 were changed from  to Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:33:53.940680+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SYT14 were set to ","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:32:56.955938+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SYT14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:32:30.909761+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SYT14 as Red List (low evidence)","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:32:30.896347+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: syt14 has been classified as Red List (Low Evidence).","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:32:01.841171+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SYT14: Rating: RED; Mode of pathogenicity: None; Publications: 21835308; Phenotypes: Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:31:24.372080+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1525","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SYT14 as ready","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:31:24.358574+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1525","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: syt14 has been classified as Red List (Low Evidence).","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:31:15.567584+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1525","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SYT14 were changed from  to Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:30:51.178039+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1524","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SYT14 were set to ","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:30:36.228511+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1523","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SYT14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:30:14.859531+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1522","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SYT14 as Red List (low evidence)","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:30:14.845774+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1522","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: syt14 has been classified as Red List (Low Evidence).","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:29:54.780739+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1521","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SYT14: Rating: RED; Mode of pathogenicity: None; Publications: 21835308; Phenotypes: Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:27:37.162693+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2273","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SYT14 were changed from Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229 to Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:27:29.523918+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2272","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SYT14 as ready","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:27:29.510483+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2272","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: syt14 has been classified as Red List (Low Evidence).","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:27:10.200545+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2272","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SYT14 were changed from  to Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:26:43.223738+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2271","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SYT14 were set to ","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:26:15.820676+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2270","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SYT14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:25:48.582037+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2269","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SYT14 as Red List (low evidence)","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:25:48.568875+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2269","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: syt14 has been classified as Red List (Low Evidence).","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:25:06.794032+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2268","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SYT14: Rating: RED; Mode of pathogenicity: None; Publications: 21835308; Phenotypes: Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SYT14","entity_type":"gene"},{"created":"2020-02-29T17:21:41.172146+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2268","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SUZ12 were changed from no OMIM number yet. to Imagawa-Matsumoto syndrome, MIM# 618786; Intellectual disability; Overgrowth","entity_name":"SUZ12","entity_type":"gene"},{"created":"2020-02-29T17:20:55.818020+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2267","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SUZ12: Rating: GREEN; Mode of pathogenicity: None; Publications: 31736240, 30019515, 28229514; Phenotypes: Imagawa-Matsumoto syndrome, MIM# 618786, Intellectual disability, Overgrowth; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SUZ12","entity_type":"gene"},{"created":"2020-02-29T17:15:52.115801+11:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SUFU as ready","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-02-29T17:15:52.102717+11:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sufu has been classified as Amber List (Moderate Evidence).","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-02-29T17:15:48.821625+11:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SUFU were changed from  to Joubert syndrome 32, MIM#617757","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-02-29T17:15:26.765890+11:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SUFU were set to ","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-02-29T17:15:04.131939+11:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SUFU was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-02-29T17:14:36.834449+11:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SUFU as Amber List (moderate evidence)","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-02-29T17:14:36.825052+11:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sufu has been classified as Amber List (Moderate Evidence).","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-02-29T17:14:07.808269+11:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SUFU: Rating: AMBER; Mode of pathogenicity: None; Publications: 28965847; Phenotypes: Joubert syndrome 32, MIM#617757; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-02-29T17:13:29.607087+11:00","panel_name":"Joubert syndrome and other cerebellar malformations","panel_id":129,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SUFU as ready","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-02-29T17:13:29.592249+11:00","panel_name":"Joubert syndrome and other cerebellar malformations","panel_id":129,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sufu has been classified as Amber List (Moderate Evidence).","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-02-29T17:13:22.231164+11:00","panel_name":"Joubert syndrome and other cerebellar malformations","panel_id":129,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SUFU were changed from  to Joubert syndrome 32, MIM#617757","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-02-29T17:12:59.568424+11:00","panel_name":"Joubert syndrome and other cerebellar malformations","panel_id":129,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SUFU were set to ","entity_name":"SUFU","entity_type":"gene"}]}