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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1901",
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"results": [
{
"created": "2020-03-18T14:44:56.611034+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UQCRQ as ready",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:44:56.597024+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcrq has been classified as Red List (Low Evidence).",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:44:53.224652+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UQCRQ were changed from to Mitochondrial complex III deficiency, nuclear type 4, MIM# 615159",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:44:38.957839+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UQCRQ as ready",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:44:38.948905+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcrq has been classified as Amber List (Moderate Evidence).",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:44:28.792726+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UQCRQ were set to ",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:44:02.685664+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UQCRQ were changed from to Mitochondrial complex III deficiency, nuclear type 4, MIM# 615159",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:43:57.558737+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UQCRQ was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:42:47.442915+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UQCRQ as Red List (low evidence)",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:42:47.424135+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcrq has been classified as Red List (Low Evidence).",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:42:19.165499+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UQCRQ: Rating: RED; Mode of pathogenicity: None; Publications: 18439546; Phenotypes: Mitochondrial complex III deficiency, nuclear type 4, MIM# 615159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:41:49.906305+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UQCRQ were set to ",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:41:22.820444+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UQCRQ was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:40:32.773753+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UQCRQ as Amber List (moderate evidence)",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:40:32.765495+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcrq has been classified as Amber List (Moderate Evidence).",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:39:55.668352+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UQCRQ: Rating: AMBER; Mode of pathogenicity: None; Publications: 18439546; Phenotypes: Mitochondrial complex III deficiency, nuclear type 4, MIM# 615159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UQCRQ",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:35:49.974869+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1761",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UQCRC2 as ready",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:35:49.966167+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1761",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcrc2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:35:32.179656+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1761",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UQCRC2 were changed from to Mitochondrial complex III deficiency, nuclear type 5, MIM# 615160",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:35:13.042156+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1760",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UQCRC2 were set to ",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:34:52.853160+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1759",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UQCRC2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:32:16.108710+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1758",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UQCRC2 as Amber List (moderate evidence)",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:32:16.095587+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1758",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcrc2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:31:55.474218+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UQCRC2 as ready",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:31:55.465296+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcrc2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:31:50.151806+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UQCRC2 were changed from to Mitochondrial complex III deficiency, nuclear type 5, MIM# 615160",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:31:24.196754+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1757",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UQCRC2: Rating: AMBER; Mode of pathogenicity: None; Publications: 28275242, 23281071; Phenotypes: Mitochondrial complex III deficiency, nuclear type 5, MIM# 615160; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:31:17.052701+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UQCRC2 were set to ",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:30:25.310788+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UQCRC2 as Amber List (moderate evidence)",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:30:25.297492+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcrc2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:30:08.591334+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1757",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UQCC3 as ready",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:30:08.582724+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1757",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcc3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:29:53.720105+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UQCRC2: Rating: AMBER; Mode of pathogenicity: None; Publications: 28275242, 23281071; Phenotypes: Mitochondrial complex III deficiency, nuclear type 5, MIM# 615160; Mode of inheritance: None",
"entity_name": "UQCRC2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:27:12.178958+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1757",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UQCC3 were changed from to Mitochondrial complex III deficiency, nuclear type 9, MIM# 616111",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:27:00.836452+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UQCC3 as ready",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:27:00.827620+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcc3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:26:38.554054+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UQCC3 were changed from to Mitochondrial complex III deficiency, nuclear type 9, MIM# 616111",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:26:09.014823+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1756",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UQCC3 were set to ",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:25:53.445645+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1755",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UQCC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:25:35.055634+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1754",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UQCC3 as Amber List (moderate evidence)",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:25:35.042287+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1754",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcc3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:25:32.075664+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UQCC3 were set to ",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:25:09.607282+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UQCC3: Rating: AMBER; Mode of pathogenicity: None; Publications: 25008109, 28804536; Phenotypes: Mitochondrial complex III deficiency, nuclear type 9, MIM# 616111; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:24:46.291289+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UQCC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:24:15.716258+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UQCC3 as Amber List (moderate evidence)",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:24:15.707692+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uqcc3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:23:39.836296+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UQCC3: Rating: AMBER; Mode of pathogenicity: None; Publications: 25008109, 28804536; Phenotypes: Mitochondrial complex III deficiency, nuclear type 9, MIM# 616111; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UQCC3",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:20:04.680777+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TXN2 as ready",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:20:04.671515+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: txn2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:19:55.042828+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TXN2 were changed from to Combined oxidative phosphorylation deficiency 29, MIM# 616811",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:19:43.475478+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TXN2 as ready",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:19:43.466352+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: txn2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:19:37.670535+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TXN2 were changed from to Combined oxidative phosphorylation deficiency 29, MIM# 616811",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:19:12.010750+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1752",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TXN2 were set to ",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:18:46.398498+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TXN2 were set to ",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:18:43.822618+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1751",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TXN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:18:21.820956+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1750",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TXN2 as Amber List (moderate evidence)",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:18:21.809738+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1750",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: txn2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:18:00.263071+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TXN2: Rating: AMBER; Mode of pathogenicity: None; Publications: 26626369, 12529397; Phenotypes: Combined oxidative phosphorylation deficiency 29, MIM# 616811; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:17:55.740345+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TXN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:17:10.801518+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TXN2 as Amber List (moderate evidence)",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:17:10.786907+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: txn2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:16:41.531595+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TXN2: Rating: AMBER; Mode of pathogenicity: None; Publications: 26626369, 12529397; Phenotypes: Combined oxidative phosphorylation deficiency 29, MIM# 616811; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TXN2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:13:16.228491+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TARS2 as ready",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:13:16.215253+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tars2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:13:03.183705+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TARS2 were changed from to Combined oxidative phosphorylation deficiency 21, MIM# 615918",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:12:49.712933+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TARS2 were set to ",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:12:35.155265+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:12:21.843463+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TARS2 as Amber List (moderate evidence)",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:12:21.829923+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tars2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:12:01.438984+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TARS2: Rating: AMBER; Mode of pathogenicity: None; Publications: 24827421, 26811336; Phenotypes: Combined oxidative phosphorylation deficiency 21, MIM# 615918; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:11:10.533004+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TARS2 were changed from to Combined oxidative phosphorylation deficiency 21, MIM# 615918",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:08:01.163345+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TARS2 were set to ",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:07:36.957892+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:07:13.121912+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TARS2 as Amber List (moderate evidence)",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:07:13.108378+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tars2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T14:06:40.238943+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TARS2: Rating: AMBER; Mode of pathogenicity: None; Publications: 24827421, 26811336; Phenotypes: Combined oxidative phosphorylation deficiency 21, MIM# 615918; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TARS2",
"entity_type": "gene"
},
{
"created": "2020-03-18T13:00:28.105673+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STAT2 as ready",
"entity_name": "STAT2",
"entity_type": "gene"
},
{
"created": "2020-03-18T13:00:28.091457+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stat2 has been classified as Green List (High Evidence).",
"entity_name": "STAT2",
"entity_type": "gene"
},
{
"created": "2020-03-18T13:00:22.647852+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STAT2 were changed from to Immunodeficiency 44, MIM# 616636",
"entity_name": "STAT2",
"entity_type": "gene"
},
{
"created": "2020-03-18T13:00:00.245611+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.173",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STAT2 were set to ",
"entity_name": "STAT2",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:59:36.974546+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: STAT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STAT2",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:59:08.176018+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: STAT2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23391734, 26122121; Phenotypes: Immunodeficiency 44, MIM# 616636; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STAT2",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:55:59.913974+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A38 as ready",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:55:59.905088+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a38 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:55:46.436337+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC25A38 as Green List (high evidence)",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:55:46.422732+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a38 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:55:16.459424+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC25A38 was added\ngene: SLC25A38 was added to Mitochondrial disease. Sources: Expert list\nMode of inheritance for gene: SLC25A38 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC25A38 were set to 19412178\nPhenotypes for gene: SLC25A38 were set to Anemia, sideroblastic, 2, pyridoxine-refractory, MIM#\t205950\nReview for gene: SLC25A38 was set to GREEN\nAdded comment: SLC25A38 belongs to the SLC25 family of mitochondrial carrier proteins. Multiple affected families reported together with an animal model. \nSources: Expert list",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:51:33.508477+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A32 as ready",
"entity_name": "SLC25A32",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:51:33.500158+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a32 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A32",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:51:25.216658+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC25A32 as Green List (high evidence)",
"entity_name": "SLC25A32",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:51:25.203658+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a32 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A32",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:51:07.158885+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.1744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC25A32 was added\ngene: SLC25A32 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: SLC25A32 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC25A32 were set to 26933868; 28443623\nPhenotypes for gene: SLC25A32 were set to Exercise intolerance, riboflavin-responsive, MIM# 616839\nReview for gene: SLC25A32 was set to GREEN\nAdded comment: Two unrelated families reported with functional data. Muscle biopsy showed ragged-red fibers and lipid storage mainly in type I oxidative fibers, small type II fibers, and poor immunostaining for succinate dehydrogenase (FAD-dependent mitochondrial respiratory chain complex II). Oral supplementation with riboflavin led to dramatic improvement in the clinical and biologic abnormalities. \nSources: Expert list",
"entity_name": "SLC25A32",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:50:48.781941+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.169",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A32 as ready",
"entity_name": "SLC25A32",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:50:48.768634+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.169",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a32 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A32",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:50:12.460876+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.169",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC25A32 as Green List (high evidence)",
"entity_name": "SLC25A32",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:50:12.451965+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.169",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a32 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A32",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:49:43.902162+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC25A32 was added\ngene: SLC25A32 was added to Mitochondrial disease. Sources: Expert list\nMode of inheritance for gene: SLC25A32 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC25A32 were set to 26933868; 28443623\nPhenotypes for gene: SLC25A32 were set to Exercise intolerance, riboflavin-responsive, MIM# 616839\nReview for gene: SLC25A32 was set to GREEN\nAdded comment: Two unrelated families reported with functional data. Muscle biopsy showed ragged-red fibers and lipid storage mainly in type I oxidative fibers, small type II fibers, and poor immunostaining for succinate dehydrogenase (FAD-dependent mitochondrial respiratory chain complex II). Oral supplementation with riboflavin led to dramatic improvement in the clinical and biologic abnormalities. \nSources: Expert list",
"entity_name": "SLC25A32",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:31:43.404603+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.167",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHB as ready",
"entity_name": "SDHB",
"entity_type": "gene"
},
{
"created": "2020-03-18T12:31:43.395070+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.167",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdhb has been classified as Amber List (Moderate Evidence).",
"entity_name": "SDHB",
"entity_type": "gene"
}
]
}