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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1866",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1864",
"results": [
{
"created": "2020-04-12T21:49:19.941506+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBCD as ready",
"entity_name": "TBCD",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:49:19.932657+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbcd has been classified as Green List (High Evidence).",
"entity_name": "TBCD",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:49:09.748184+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBCD were changed from to Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum, MIM#617193",
"entity_name": "TBCD",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:48:55.735044+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBCD were set to ",
"entity_name": "TBCD",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:48:23.513552+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBCD was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBCD",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:47:31.790314+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TMTC2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TMTC2",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:46:35.056683+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TMTC2 as Amber List (moderate evidence)",
"entity_name": "TMTC2",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:46:35.043332+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmtc2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TMTC2",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:45:39.869200+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UMOD as ready",
"entity_name": "UMOD",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:45:39.859272+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: umod has been classified as Green List (High Evidence).",
"entity_name": "UMOD",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:45:25.129957+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TOR1AIP1 as ready",
"entity_name": "TOR1AIP1",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:45:25.116401+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tor1aip1 has been classified as Green List (High Evidence).",
"entity_name": "TOR1AIP1",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:44:33.321172+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UPK3A as ready",
"entity_name": "UPK3A",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:44:33.307930+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: upk3a has been classified as Red List (Low Evidence).",
"entity_name": "UPK3A",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:44:32.422993+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UMOD were changed from to Glomerulocystic kidney disease with hyperuricemia and isosthenuria 609886; Hyperuricemic nephropathy, familial juvenile 1 162000; Medullary cystic kidney disease 2 603860",
"entity_name": "UMOD",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:44:06.543286+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UMOD: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Glomerulocystic kidney disease with hyperuricemia and isosthenuria 609886, Hyperuricemic nephropathy, familial juvenile 1 162000, Medullary cystic kidney disease 2 603860; Mode of inheritance: None",
"entity_name": "UMOD",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:42:30.916844+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UPK3A were changed from to CAKUT",
"entity_name": "UPK3A",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:42:08.618846+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UPK3A were set to ",
"entity_name": "UPK3A",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:41:37.808089+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UPK3A as Red List (low evidence)",
"entity_name": "UPK3A",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:41:37.799624+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: upk3a has been classified as Red List (Low Evidence).",
"entity_name": "UPK3A",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:40:50.188361+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VARS as ready",
"entity_name": "VARS",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:40:50.175396+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vars has been classified as Green List (High Evidence).",
"entity_name": "VARS",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:40:41.478090+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VARS were changed from to Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy; OMIM #617802",
"entity_name": "VARS",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:39:54.935286+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WNT10A as ready",
"entity_name": "WNT10A",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:39:54.926004+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnt10a has been classified as Green List (High Evidence).",
"entity_name": "WNT10A",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:39:50.333019+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF592 as ready",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:39:50.319065+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf592 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:39:44.100098+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WNT10A were changed from to Odontoonychodermal dysplasia; Schopf-Schulz-Passarge syndrome; Tooth agenesis, selective, 4",
"entity_name": "WNT10A",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:39:27.212100+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WNT10A were set to ",
"entity_name": "WNT10A",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:39:11.274722+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WNT10A was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "WNT10A",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:38:16.825415+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF592 were changed from to SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:37:52.914209+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZNF592 were set to ",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:37:27.778006+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.103",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZNF592 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:36:52.285712+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZNF592 as Red List (low evidence)",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:36:52.272502+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf592 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:36:19.625498+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF592 as ready",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:36:19.616906+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf592 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:36:11.485452+10:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZNF592: Rating: RED; Mode of pathogenicity: None; Publications: 20531441, 26123727; Phenotypes: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:35:42.649730+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF592 were changed from to SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:34:42.877957+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZNF592 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:33:51.940629+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZNF592 were set to ",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:33:37.776973+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZNF592 as Red List (low evidence)",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:33:37.763650+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf592 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF592",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:32:29.657813+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLIC5 as ready",
"entity_name": "CLIC5",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:32:29.644683+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clic5 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CLIC5",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:31:40.302415+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GNB2 as ready",
"entity_name": "GNB2",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:31:40.293123+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gnb2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GNB2",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:30:58.302396+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MIR96 as ready",
"entity_name": "MIR96",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:30:58.289099+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mir96 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MIR96",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:30:28.835126+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYL1 as ready",
"entity_name": "MYL1",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:30:28.826553+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myl1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MYL1",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:29:19.145159+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: APOL1 as ready",
"entity_name": "APOL1",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:29:19.131974+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: apol1 has been classified as Red List (Low Evidence).",
"entity_name": "APOL1",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:28:41.015872+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ARHGEF6 as ready",
"entity_name": "ARHGEF6",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:28:41.007402+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arhgef6 has been classified as Red List (Low Evidence).",
"entity_name": "ARHGEF6",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:27:55.564104+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CEP85L as ready",
"entity_name": "CEP85L",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:27:55.550891+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep85l has been classified as Green List (High Evidence).",
"entity_name": "CEP85L",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:27:46.374899+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CEP85L as Green List (high evidence)",
"entity_name": "CEP85L",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:27:46.365836+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep85l has been classified as Green List (High Evidence).",
"entity_name": "CEP85L",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:26:27.601001+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MIEF2 as ready",
"entity_name": "MIEF2",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:26:27.587819+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mief2 has been classified as Red List (Low Evidence).",
"entity_name": "MIEF2",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:25:48.534344+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POLE2 as ready",
"entity_name": "POLE2",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:25:48.525617+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pole2 has been classified as Red List (Low Evidence).",
"entity_name": "POLE2",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:25:19.581205+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTCD1 as ready",
"entity_name": "PTCD1",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:25:19.567575+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ptcd1 has been classified as Red List (Low Evidence).",
"entity_name": "PTCD1",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:24:39.473389+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TFAM as ready",
"entity_name": "TFAM",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:24:39.461917+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tfam has been classified as Amber List (Moderate Evidence).",
"entity_name": "TFAM",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:24:30.451604+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TFAM as Amber List (moderate evidence)",
"entity_name": "TFAM",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:24:30.438782+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tfam has been classified as Amber List (Moderate Evidence).",
"entity_name": "TFAM",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:22:38.680842+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NME3 as ready",
"entity_name": "NME3",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:22:38.671531+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nme3 has been classified as Red List (Low Evidence).",
"entity_name": "NME3",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:22:27.943706+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NME3 was added\ngene: NME3 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: NME3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NME3 were set to 30587587\nPhenotypes for gene: NME3 were set to Hypotonia; Neurodegeneration; Abnormal mitochondrial dynamics\nReview for gene: NME3 was set to RED\nAdded comment: Single individual reported. NME3 is a mitochondrial outer-membrane protein capable of interacting with MFN1/2, and its depletion causes dysfunction in mitochondrial dynamics \nSources: Expert list",
"entity_name": "NME3",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:20:48.440100+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.348",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NME3 as ready",
"entity_name": "NME3",
"entity_type": "gene"
},
{
"created": "2020-04-12T21:20:48.431029+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.348",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nme3 has been classified as Red List (Low Evidence).",
"entity_name": "NME3",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:31:15.548457+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.348",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NME3 was added\ngene: NME3 was added to Mitochondrial disease. Sources: Expert list\nMode of inheritance for gene: NME3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NME3 were set to 30587587\nPhenotypes for gene: NME3 were set to Hypotonia; Neurodegeneration; Abnormal mitochondrial dynamics\nReview for gene: NME3 was set to RED\nAdded comment: Single individual reported. NME3 is a mitochondrial outer-membrane protein capable of interacting with MFN1/2, and its depletion causes dysfunction in mitochondrial dynamics. \nSources: Expert list",
"entity_name": "NME3",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:22:11.135948+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRPS28 as ready",
"entity_name": "MRPS28",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:22:11.122799+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps28 has been classified as Red List (Low Evidence).",
"entity_name": "MRPS28",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:21:57.674974+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MRPS28 was added\ngene: MRPS28 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: MRPS28 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MRPS28 were set to 30566640\nPhenotypes for gene: MRPS28 were set to Intrauterine growth retardation; developmental delay; dysmorphism\nReview for gene: MRPS28 was set to RED\nAdded comment: Single individual reported. \nSources: Expert list",
"entity_name": "MRPS28",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:20:22.917608+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.347",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRPS28 as ready",
"entity_name": "MRPS28",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:20:22.904332+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.347",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps28 has been classified as Red List (Low Evidence).",
"entity_name": "MRPS28",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:20:13.814639+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.347",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MRPS28 was added\ngene: MRPS28 was added to Mitochondrial disease. Sources: Expert list\nMode of inheritance for gene: MRPS28 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MRPS28 were set to 30566640\nPhenotypes for gene: MRPS28 were set to Intrauterine growth retardation; developmental delay; dysmorphism\nReview for gene: MRPS28 was set to RED\nAdded comment: Single individual reported. \nSources: Expert list",
"entity_name": "MRPS28",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:17:15.012306+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRPS25 as ready",
"entity_name": "MRPS25",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:17:14.996221+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps25 has been classified as Red List (Low Evidence).",
"entity_name": "MRPS25",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:17:05.497475+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MRPS25 was added\ngene: MRPS25 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: MRPS25 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MRPS25 were set to 31039582\nPhenotypes for gene: MRPS25 were set to Dyskinetic cerebral palsy; Mitochondrial myopathy; Partial agenesis of the corpus callosum\nReview for gene: MRPS25 was set to RED\nAdded comment: Single individual reported. \nSources: Expert list",
"entity_name": "MRPS25",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:15:34.327173+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.346",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRPS25 as ready",
"entity_name": "MRPS25",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:15:34.314390+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.346",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps25 has been classified as Red List (Low Evidence).",
"entity_name": "MRPS25",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:15:26.892004+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.346",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MRPS25 was added\ngene: MRPS25 was added to Mitochondrial disease. Sources: Expert list\nMode of inheritance for gene: MRPS25 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MRPS25 were set to 31039582\nPhenotypes for gene: MRPS25 were set to Dyskinetic cerebral palsy; Mitochondrial myopathy; Partial agenesis of the corpus callosum\nReview for gene: MRPS25 was set to RED\nAdded comment: Single individual reported. \nSources: Expert list",
"entity_name": "MRPS25",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:12:09.823358+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MRPS23 were changed from Hepatic disease; Combined respiratory chain complex deficiencies to Hepatic disease; Combined respiratory chain complex deficienciesHepatic disease; Combined respiratory chain complex deficiencies; Cardiomyopathy; Tubulopathy; Lactic acidosis; Structural brain abnormalities",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:11:49.060993+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MRPS23 were set to 26741492",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:11:21.062911+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MRPS23 as Green List (high evidence)",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:11:21.049881+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps23 has been classified as Green List (High Evidence).",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:11:00.551586+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2173",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:10:52.822127+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2173",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: MRPS23: Added comment: Four families reported.; Changed rating: GREEN; Changed publications: 26741492, 17873122, 25663021, 28752220; Changed phenotypes: Hepatic disease, Combined respiratory chain complex deficiencies, Cardiomyopathy, Tubulopathy, Lactic acidosis, Structural brain abnormalities",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:09:54.863181+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.345",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MRPS23 were changed from Hepatic disease; Combined respiratory chain complex deficiencies to Hepatic disease; Combined respiratory chain complex deficiencies; Cardiomyopathy; Tubulopathy; Lactic acidosis; Structural brain abnormalities",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:09:02.989477+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.344",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MRPS23 were set to 26741492",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:08:30.196675+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.343",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MRPS23 as Green List (high evidence)",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:08:30.188055+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.343",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps23 has been classified as Green List (High Evidence).",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:07:50.949729+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: MRPS23: Changed rating: GREEN",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:07:43.256384+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Single family reported.; to: Four families reported.",
"entity_name": "MRPS23",
"entity_type": "gene"
},
{
"created": "2020-04-12T18:07:32.976850+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: MRPS23: Changed publications: 26741492, 17873122, 25663021, 28752220; Changed phenotypes: Hepatic disease, Combined respiratory chain complex deficiencies, Cardiomyopathy, Tubulopathy, Lactic acidosis, Structural brain abnormalities",
"entity_name": "MRPS23",
"entity_type": "gene"
}
]
}