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{
"count": 220314,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1341",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1339",
"results": [
{
"created": "2021-04-24T14:37:52.901254+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SALL4 were changed from to Duane-radial ray syndrome, MIM# 607323; MONDO:0011812; IVIC syndrome, MIM# 147750; MONDO:0007836",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:37:28.847113+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SALL4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:36:58.974042+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SALL4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Duane-radial ray syndrome, MIM# 607323, MONDO:0011812, IVIC syndrome, MIM# 147750, MONDO:0007836; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:34:51.451266+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7322",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SALL1 as ready",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:34:51.437451+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7322",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sall1 has been classified as Green List (High Evidence).",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:34:42.970640+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7322",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SALL1 were changed from to Townes-Brocks syndrome 1, MIM#107480; MONDO:0054581",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:34:22.373850+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7321",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SALL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:34:01.258157+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7320",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SALL1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Townes-Brocks syndrome 1, MIM#107480, MONDO:0054581; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:33:09.723525+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SALL1 as ready",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:33:09.711435+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sall1 has been classified as Green List (High Evidence).",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:33:06.169805+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SALL1 were changed from to Townes-Brocks syndrome 1, MIM#107480; MONDO:0054581",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:32:31.218323+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SALL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:32:05.071706+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SALL1: Added comment: Well established gene-disease association.; Changed phenotypes: Townes-Brocks syndrome 1, MIM#107480, MONDO:0054581",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:31:07.912384+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SALL1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Townes-Brocks syndrome 1, 107480; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SALL1",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:30:35.366930+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS7 as ready",
"entity_name": "RPS7",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:30:35.357141+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps7 has been classified as Green List (High Evidence).",
"entity_name": "RPS7",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:30:31.236501+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS7 were changed from to Diamond-Blackfan anaemia 8, MIM# 612563; MONDO:0012939",
"entity_name": "RPS7",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:30:03.597192+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPS7 were set to ",
"entity_name": "RPS7",
"entity_type": "gene"
},
{
"created": "2021-04-24T14:29:38.385653+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS7 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS7",
"entity_type": "gene"
},
{
"created": "2021-04-24T12:00:38.689722+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS26 as ready",
"entity_name": "RPS26",
"entity_type": "gene"
},
{
"created": "2021-04-24T12:00:38.679952+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps26 has been classified as Green List (High Evidence).",
"entity_name": "RPS26",
"entity_type": "gene"
},
{
"created": "2021-04-24T12:00:33.510467+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS26 were changed from to Diamond-Blackfan anaemia 10, MIM# 613309; MONDO:0013217",
"entity_name": "RPS26",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:58:41.944430+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPS26 were set to ",
"entity_name": "RPS26",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:58:19.813673+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS26 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS26",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:57:16.039041+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS24 as ready",
"entity_name": "RPS24",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:57:16.029813+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps24 has been classified as Green List (High Evidence).",
"entity_name": "RPS24",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:57:03.471448+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS24 were changed from to Diamond-blackfan anaemia 3, MIM# 610629; MONDO:0012529",
"entity_name": "RPS24",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:56:32.542431+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPS24 were set to ",
"entity_name": "RPS24",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:56:03.416876+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS24 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS24",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:55:38.756671+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: At least 3 unrelated individuals reported.; to: At least 3 unrelated individuals reported. Thumb abnormalities are a feature.",
"entity_name": "RPS24",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:55:27.246000+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: RPS24: Changed phenotypes: Diamond-blackfan anaemia 3, MIM# 610629, MONDO:0012529",
"entity_name": "RPS24",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:54:52.077660+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS19 were changed from Diamond-Blackfan anemia 1, MIM# 105650; MONDO:0007110 to Diamond-Blackfan anaemia 1, MIM# 105650; MONDO:0007110",
"entity_name": "RPS19",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:54:06.442557+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.217",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS17 were changed from Diamond-Blackfan anemia 4, MIM#\t612527 to Diamond-Blackfan anaemia 4, MIM#\t612527; MONDO:0012924",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:53:20.764037+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7320",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS17 were changed from Diamond-Blackfan anemia 4, MIM# 612527 to Diamond-Blackfan anaemia 4, MIM# 612527; MONDO:0012924",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:52:42.086387+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS17 were changed from Diamond-Blackfan anemia 4, MIM# 612527 to Diamond-Blackfan anaemia 4, MIM# 612527; MONDO:0012924",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:51:44.361714+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS10 as ready",
"entity_name": "RPS10",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:51:44.351887+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps10 has been classified as Green List (High Evidence).",
"entity_name": "RPS10",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:51:34.025297+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS10 were changed from to Diamond-Blackfan anemia 9, MIM# 613308; MONDO:0013216",
"entity_name": "RPS10",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:50:52.266521+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPS10 were set to ",
"entity_name": "RPS10",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:50:23.255316+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS10 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS10",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:49:47.941810+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPL5 as ready",
"entity_name": "RPL5",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:49:47.926510+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rpl5 has been classified as Green List (High Evidence).",
"entity_name": "RPL5",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:49:44.696275+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPL5 were changed from to Diamond-Blackfan anaemia 6, MIM# 612561; MONDO:0012937",
"entity_name": "RPL5",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:49:13.541251+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPL5 were set to ",
"entity_name": "RPL5",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:48:49.808813+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPL5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPL5",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:48:21.013843+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPL35A as ready",
"entity_name": "RPL35A",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:48:21.003101+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rpl35a has been classified as Green List (High Evidence).",
"entity_name": "RPL35A",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:48:09.083154+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.216",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPL35A were changed from Diamond-Blackfan anemia 5, MIM# 612528 to Diamond-Blackfan anemia 5, MIM# 612528; MONDO:0012925",
"entity_name": "RPL35A",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:47:40.640182+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: RPL35A.",
"entity_name": "RPL35A",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:47:24.197973+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7319",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPL35A were changed from Diamond-Blackfan anemia 5, MIM# 612528 to Diamond-Blackfan anemia 5, MIM# 612528; MONDO:0012925",
"entity_name": "RPL35A",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:47:06.220525+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7318",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: RPL35A: Changed phenotypes: Diamond-Blackfan anemia 5, MIM# 612528, MONDO:0012925",
"entity_name": "RPL35A",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:47:01.910845+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPL35A were changed from Diamond-Blackfan anaemia 5, MIM# 612528 to Diamond-Blackfan anaemia 5, MIM# 612528; MONDO:0012925",
"entity_name": "RPL35A",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:46:25.105751+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPL35A were changed from to Diamond-Blackfan anaemia 5, MIM# 612528",
"entity_name": "RPL35A",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:46:00.474048+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPL35A were set to ",
"entity_name": "RPL35A",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:45:35.336833+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPL35A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPL35A",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:45:07.704793+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: RPL35A.",
"entity_name": "RPL35A",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:44:38.817144+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Well established gene-disease association.; to: Well established gene-disease association, thumb abnormalities are a feature.",
"entity_name": "RPL11",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:44:24.567213+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPL11 as ready",
"entity_name": "RPL11",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:44:24.557251+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rpl11 has been classified as Green List (High Evidence).",
"entity_name": "RPL11",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:44:21.373275+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPL11 were changed from to Diamond-Blackfan anaemia 7, MIM# 612562; MONDO:0012938",
"entity_name": "RPL11",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:43:49.603433+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPL11 were set to ",
"entity_name": "RPL11",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:43:27.832109+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPL11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPL11",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:42:26.618653+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PALB2 as ready",
"entity_name": "PALB2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:42:26.609024+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: palb2 has been classified as Green List (High Evidence).",
"entity_name": "PALB2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:41:59.484352+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PALB2 were changed from to Fanconi anaemia, complementation group N, MIM# 610832",
"entity_name": "PALB2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:41:28.921855+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PALB2 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PALB2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:41:13.578479+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PALB2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PALB2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:39:12.593061+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCI as ready",
"entity_name": "FANCI",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:39:12.583244+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fanci has been classified as Green List (High Evidence).",
"entity_name": "FANCI",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:38:52.155920+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCL as ready",
"entity_name": "FANCL",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:38:52.114872+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fancl has been classified as Green List (High Evidence).",
"entity_name": "FANCL",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:38:49.533222+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCL were changed from to Fanconi anemia, complementation group L, MIM# 614083; MONDO:0013566",
"entity_name": "FANCL",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:38:34.324605+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCI were changed from to Fanconi anemia, complementation group I, MIM# 609053; MONDO:0012186",
"entity_name": "FANCI",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:38:09.048102+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FANCL were set to ",
"entity_name": "FANCL",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:37:51.908441+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FANCI were set to ",
"entity_name": "FANCI",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:37:31.546570+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FANCL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCL",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:37:11.170058+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FANCI was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCI",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:36:43.329891+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCF as ready",
"entity_name": "FANCF",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:36:43.315433+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fancf has been classified as Green List (High Evidence).",
"entity_name": "FANCF",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:36:37.127576+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCG as ready",
"entity_name": "FANCG",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:36:37.114956+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fancg has been classified as Green List (High Evidence).",
"entity_name": "FANCG",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:36:28.257750+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCG were changed from to Fanconi anaemia, complementation group G, MIM# 614082; MONDO:0013565",
"entity_name": "FANCG",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:35:58.106932+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCF were changed from to Fanconi anaemia, complementation group F 603467; MONDO:0011325",
"entity_name": "FANCF",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:35:42.845597+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FANCG were set to ",
"entity_name": "FANCG",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:35:22.079376+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.107",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FANCF were set to ",
"entity_name": "FANCF",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:35:07.160446+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.107",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FANCG was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCG",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:34:43.606769+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FANCF was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCF",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:34:12.859305+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCE as ready",
"entity_name": "FANCE",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:34:12.849246+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fance has been classified as Green List (High Evidence).",
"entity_name": "FANCE",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:34:01.410396+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCE were changed from to Fanconi anaemia, complementation group E, MIM# 600901; MONDO:0010953",
"entity_name": "FANCE",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:33:33.026295+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FANCE were set to ",
"entity_name": "FANCE",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:33:08.721079+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.103",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FANCE was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCE",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:32:13.201682+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.7318",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCD2 were changed from Fanconi anemia, complementation group D2, MIM#227646 to Fanconi anemia, complementation group D2, MIM#227646; MONDO:0009214",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:31:45.835517+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCD2 as ready",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:31:45.825825+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fancd2 has been classified as Green List (High Evidence).",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:31:38.879535+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCD2 were changed from Fanconi anaemia, complementation group D2, MIM# 227646 to Fanconi anaemia, complementation group D2, MIM# 227646; MONDO:0009214",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:31:06.721379+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCD2 were changed from to Fanconi anaemia, complementation group D2, MIM# 227646",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:30:37.492417+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FANCD2 were set to ",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:30:14.637469+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FANCD2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2021-04-24T11:29:40.744222+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCC as ready",
"entity_name": "FANCC",
"entity_type": "gene"
}
]
}