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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1917",
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"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"
}
]
}