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{
"count": 221272,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=704",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=702",
"results": [
{
"created": "2022-11-03T07:09:58.851947+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.760",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PEX3 as Red List (low evidence)",
"entity_name": "PEX3",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:09:58.843352+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.760",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex3 has been classified as Red List (Low Evidence).",
"entity_name": "PEX3",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:09:25.598688+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.759",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX26 as ready",
"entity_name": "PEX26",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:09:25.583659+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.759",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex26 has been classified as Red List (Low Evidence).",
"entity_name": "PEX26",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:09:19.535837+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.759",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX26 were changed from Zellweger syndrome to Peroxisome biogenesis disorder 7A (Zellweger) MIM#614872",
"entity_name": "PEX26",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:09:09.956221+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.758",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PEX26 as Red List (low evidence)",
"entity_name": "PEX26",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:09:09.944325+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.758",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex26 has been classified as Red List (Low Evidence).",
"entity_name": "PEX26",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:08:15.847415+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.757",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX2 as ready",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:08:15.833696+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.757",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex2 has been classified as Red List (Low Evidence).",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:08:11.915633+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.757",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX2 were changed from Zellweger syndrome to Peroxisome biogenesis disorder 5A (Zellweger) MIM#614866",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:08:02.493095+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.756",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PEX2 as Red List (low evidence)",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:08:02.481444+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.756",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex2 has been classified as Red List (Low Evidence).",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:07:24.218408+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.755",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX13 as ready",
"entity_name": "PEX13",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:07:24.209525+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.755",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex13 has been classified as Red List (Low Evidence).",
"entity_name": "PEX13",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:07:20.164027+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.755",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX13 were changed from Zellweger syndrome to Peroxisome biogenesis disorder 11A (Zellweger) (MIM#614883)",
"entity_name": "PEX13",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:06:57.027415+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.754",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PEX13 as Red List (low evidence)",
"entity_name": "PEX13",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:06:57.016802+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.754",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex13 has been classified as Red List (Low Evidence).",
"entity_name": "PEX13",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:06:22.075498+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX12 as ready",
"entity_name": "PEX12",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:06:22.066303+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex12 has been classified as Red List (Low Evidence).",
"entity_name": "PEX12",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:05:41.163328+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX12 were changed from Zellweger syndrome to Peroxisome biogenesis disorder 3A (Zellweger) (MIM#614859)",
"entity_name": "PEX12",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:05:31.651125+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.752",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PEX12 as Red List (low evidence)",
"entity_name": "PEX12",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:05:31.633240+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.752",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex12 has been classified as Red List (Low Evidence).",
"entity_name": "PEX12",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:04:19.882051+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.751",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX10 as ready",
"entity_name": "PEX10",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:04:19.873725+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.751",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex10 has been classified as Red List (Low Evidence).",
"entity_name": "PEX10",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:04:16.222272+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.751",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX10 were changed from Zellweger syndrome to Peroxisome biogenesis disorder 6A (Zellweger) (MIM#614870)",
"entity_name": "PEX10",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:04:05.357060+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.750",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PEX10 as Red List (low evidence)",
"entity_name": "PEX10",
"entity_type": "gene"
},
{
"created": "2022-11-03T07:04:05.348781+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.750",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex10 has been classified as Red List (Low Evidence).",
"entity_name": "PEX10",
"entity_type": "gene"
},
{
"created": "2022-11-03T06:58:35.031234+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: CYP27A1.",
"entity_name": "CYP27A1",
"entity_type": "gene"
},
{
"created": "2022-11-03T06:57:51.097517+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: PCBD1.",
"entity_name": "PCBD1",
"entity_type": "gene"
},
{
"created": "2022-11-02T20:09:33.694788+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: UROD.",
"entity_name": "UROD",
"entity_type": "gene"
},
{
"created": "2022-11-02T20:08:58.188716+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.165",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GNPTAB as ready",
"entity_name": "GNPTAB",
"entity_type": "gene"
},
{
"created": "2022-11-02T20:08:58.177338+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.165",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gnptab has been classified as Green List (High Evidence).",
"entity_name": "GNPTAB",
"entity_type": "gene"
},
{
"created": "2022-11-02T20:08:52.244835+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.165",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GNPTAB as Green List (high evidence)",
"entity_name": "GNPTAB",
"entity_type": "gene"
},
{
"created": "2022-11-02T20:08:52.233801+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.165",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gnptab has been classified as Green List (High Evidence).",
"entity_name": "GNPTAB",
"entity_type": "gene"
},
{
"created": "2022-11-02T20:07:51.996205+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GNPNAT1 as ready",
"entity_name": "GNPNAT1",
"entity_type": "gene"
},
{
"created": "2022-11-02T20:07:51.987167+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gnpnat1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GNPNAT1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:10:58.186680+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GNPNAT1 as Amber List (moderate evidence)",
"entity_name": "GNPNAT1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:10:58.178222+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gnpnat1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GNPNAT1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:10:00.488127+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PAX6 as ready",
"entity_name": "PAX6",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:10:00.478388+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pax6 has been classified as Red List (Low Evidence).",
"entity_name": "PAX6",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:09:55.282447+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PAX6 were changed from Aniridia to Aniridia, OMIM 106210",
"entity_name": "PAX6",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:09:44.193408+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PAX6 as Red List (low evidence)",
"entity_name": "PAX6",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:09:44.184143+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pax6 has been classified as Red List (Low Evidence).",
"entity_name": "PAX6",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:09:32.435474+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PAX6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "PAX6",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:09:16.157060+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: PAX6.",
"entity_name": "PAX6",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:08:40.617061+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PAX3 as ready",
"entity_name": "PAX3",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:08:40.606823+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pax3 has been classified as Green List (High Evidence).",
"entity_name": "PAX3",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:08:37.132417+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PAX3 were changed from Waardenburg syndrome to Waardenburg syndrome, type 1, OMIM 193500",
"entity_name": "PAX3",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:08:01.941443+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PANK2 as ready",
"entity_name": "PANK2",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:08:01.932457+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pank2 has been classified as Red List (Low Evidence).",
"entity_name": "PANK2",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:07:58.372700+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PANK2 were changed from Neurodegeneration with brain iron accumulation 1 to Neurodegeneration with brain iron accumulation 1 (aka Hallervorden-Spatz disease), OMIM 234200",
"entity_name": "PANK2",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:07:45.567938+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PANK2 as Red List (low evidence)",
"entity_name": "PANK2",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:07:45.559508+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pank2 has been classified as Red List (Low Evidence).",
"entity_name": "PANK2",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:07:02.339533+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: PALB2.",
"entity_name": "PALB2",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:06:33.254204+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PAK3 as ready",
"entity_name": "PAK3",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:06:33.245777+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pak3 has been classified as Red List (Low Evidence).",
"entity_name": "PAK3",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:06:29.055618+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PAK3 were changed from Mental retardation syndrome, X-linked to Mental retardation syndrome, X-linked 30, MIM#300558",
"entity_name": "PAK3",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:06:11.917553+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PAK3 as Red List (low evidence)",
"entity_name": "PAK3",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:06:11.908431+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pak3 has been classified as Red List (Low Evidence).",
"entity_name": "PAK3",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:05:42.091558+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: P2RY12 as ready",
"entity_name": "P2RY12",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:05:42.082326+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: p2ry12 has been classified as Red List (Low Evidence).",
"entity_name": "P2RY12",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:05:32.766979+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: P2RY12 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "P2RY12",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:05:17.043224+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: P2RY12 as Red List (low evidence)",
"entity_name": "P2RY12",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:05:17.034325+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: p2ry12 has been classified as Red List (Low Evidence).",
"entity_name": "P2RY12",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:04:37.798505+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX1 as ready",
"entity_name": "PEX1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:04:37.786210+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex1 has been classified as Red List (Low Evidence).",
"entity_name": "PEX1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:04:34.515888+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX1 were changed from Zellweger syndrome to Peroxisome biogenesis disorder 1A (Zellweger), MIM#\t214100",
"entity_name": "PEX1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:04:12.119285+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.739",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PEX1 as Red List (low evidence)",
"entity_name": "PEX1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:04:12.110174+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.739",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex1 has been classified as Red List (Low Evidence).",
"entity_name": "PEX1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:03:47.769346+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDHX as ready",
"entity_name": "PDHX",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:03:47.760729+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pdhx has been classified as Green List (High Evidence).",
"entity_name": "PDHX",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:03:43.932553+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDHX were changed from Pyruvate dehydrogenase complex deficiency to Lactic acidaemia due to PDX1 deficiency, MIM# 245349",
"entity_name": "PDHX",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:03:33.277021+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.737",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDHX were set to ",
"entity_name": "PDHX",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:03:18.347324+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PDHX: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Lactic acidaemia due to PDX1 deficiency, MIM# 245349; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDHX",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:02:34.971111+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDHA1 as ready",
"entity_name": "PDHA1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:02:34.958555+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pdha1 has been classified as Green List (High Evidence).",
"entity_name": "PDHA1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:02:31.505962+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDHA1 were changed from Pyruvate dehydrogenase deficiency to Pyruvate dehydrogenase E1-alpha deficiency, MIM# 312170",
"entity_name": "PDHA1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:02:17.702189+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PDHA1 was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "PDHA1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:02:02.706726+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.734",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "commented on gene: PDHA1: To be reported in females.",
"entity_name": "PDHA1",
"entity_type": "gene"
},
{
"created": "2022-11-02T19:00:05.580818+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.734",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PDHA1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pyruvate dehydrogenase E1-alpha deficiency, MIM# 312170; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "PDHA1",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:59:16.938029+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.734",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PC as ready",
"entity_name": "PC",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:59:16.926832+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.734",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pc has been classified as Green List (High Evidence).",
"entity_name": "PC",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:59:13.667564+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.734",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PC were changed from Pyruvate carboxylase deficiency to Pyruvate carboxylase deficiency, MIM# 266150",
"entity_name": "PC",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:59:02.903207+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PC were set to ",
"entity_name": "PC",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:58:50.419560+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.732",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PC: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pyruvate carboxylase deficiency, MIM# 266150; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PC",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:57:51.631764+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.732",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PAX8 as ready",
"entity_name": "PAX8",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:57:51.623559+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.732",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pax8 has been classified as Green List (High Evidence).",
"entity_name": "PAX8",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:57:44.537981+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.732",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PAX8 were changed from Hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia to Hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia, MIM#\t218700",
"entity_name": "PAX8",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:57:23.212081+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.731",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PAX8 were set to ",
"entity_name": "PAX8",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:56:14.169222+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.730",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: NPC2.",
"entity_name": "NPC2",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:54:31.537159+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYCBP2 as ready",
"entity_name": "MYCBP2",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:54:31.527502+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mycbp2 has been classified as Green List (High Evidence).",
"entity_name": "MYCBP2",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:54:28.254724+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYCBP2 were changed from neurodevelopmental spectrum disorder with corpus callosum defects to Neurodevelopmental disorder, MONDO:0700092, MYCBP2-related; corpus callosum abnormalities",
"entity_name": "MYCBP2",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:53:12.574451+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MYCBP2 as Green List (high evidence)",
"entity_name": "MYCBP2",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:53:12.566202+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mycbp2 has been classified as Green List (High Evidence).",
"entity_name": "MYCBP2",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:47:20.432053+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.730",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC16A2 as Amber List (moderate evidence)",
"entity_name": "SLC16A2",
"entity_type": "gene"
},
{
"created": "2022-11-02T18:47:20.422364+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.730",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc16a2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SLC16A2",
"entity_type": "gene"
},
{
"created": "2022-11-02T17:56:41.362410+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.729",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CYP27A1 as Red List (low evidence)",
"entity_name": "CYP27A1",
"entity_type": "gene"
},
{
"created": "2022-11-02T17:56:41.351229+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.729",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp27a1 has been classified as Red List (Low Evidence).",
"entity_name": "CYP27A1",
"entity_type": "gene"
},
{
"created": "2022-11-02T17:56:32.724087+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.728",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review was removed from gene: CYP27A1.",
"entity_name": "CYP27A1",
"entity_type": "gene"
}
]
}