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{
"count": 220941,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1622",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1620",
"results": [
{
"created": "2020-09-01T08:38:34.234089+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.249",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: YRDC as Green List (high evidence)",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:38:34.226186+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.249",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: yrdc has been classified as Green List (High Evidence).",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:38:32.071626+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: YRDC as ready",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:38:32.060468+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: yrdc has been classified as Green List (High Evidence).",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:38:24.372017+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: YRDC as Green List (high evidence)",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:38:24.363073+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: yrdc has been classified as Green List (High Evidence).",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:38:16.092015+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4059",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: YRDC as ready",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:38:16.082378+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4059",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: yrdc has been classified as Green List (High Evidence).",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:37:55.979755+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.248",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: YRDC was added\ngene: YRDC was added to Microcephaly. Sources: Literature\nMode of inheritance for gene: YRDC was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: YRDC were set to 31481669\nPhenotypes for gene: YRDC were set to Galloway-Mowat syndrome\nReview for gene: YRDC was set to GREEN\nAdded comment: Three individuals from two unrelated families with typical features of Galloway-Mowat syndrome including proteinuria, microcephaly, developmental delay and brain malformations. Supportive functional data. \nSources: Literature",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:37:52.081647+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4059",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: YRDC as Green List (high evidence)",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:37:52.072676+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4059",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: yrdc has been classified as Green List (High Evidence).",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:37:48.950389+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: YRDC was added\ngene: YRDC was added to Proteinuria. Sources: Literature\nMode of inheritance for gene: YRDC was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: YRDC were set to 31481669\nPhenotypes for gene: YRDC were set to Galloway-Mowat syndrome\nReview for gene: YRDC was set to GREEN\nAdded comment: Three individuals from two unrelated families with typical features of Galloway-Mowat syndrome including proteinuria, microcephaly, developmental delay and brain malformations. Supportive functional data. \nSources: Literature",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T08:36:52.686410+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4058",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: YRDC was added\ngene: YRDC was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: YRDC was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: YRDC were set to 31481669\nPhenotypes for gene: YRDC were set to Galloway-Mowat syndrome\nReview for gene: YRDC was set to GREEN\nAdded comment: Three individuals from two unrelated families with typical features of Galloway-Mowat syndrome including proteinuria, microcephaly, developmental delay and brain malformations. Supportive functional data. \nSources: Literature",
"entity_name": "YRDC",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:06:40.539126+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4057",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GON7 as ready",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:06:40.527328+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4057",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gon7 has been classified as Green List (High Evidence).",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:06:33.955979+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4057",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GON7 as Green List (high evidence)",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:06:33.947949+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4057",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gon7 has been classified as Green List (High Evidence).",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:06:19.124247+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4056",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GON7 was added\ngene: GON7 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: GON7 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GON7 were set to 31481669\nPhenotypes for gene: GON7 were set to Galloway-Mowat syndrome\nReview for gene: GON7 was set to GREEN\nAdded comment: 11 individuals from 5 families. Four of the families had the same homozygous variant, shared haplotype suggestive of founder effect. Clinical features included proteinuria, microcephaly, brain malformations and developmental delay. Supportive functional data. \nSources: Literature",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:04:55.145703+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.247",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GON7 as ready",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:04:55.135589+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.247",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gon7 has been classified as Green List (High Evidence).",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:04:50.673731+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.247",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GON7 as Green List (high evidence)",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:04:50.663895+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.247",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gon7 has been classified as Green List (High Evidence).",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:04:23.797154+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.246",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GON7 was added\ngene: GON7 was added to Microcephaly. Sources: Literature\nMode of inheritance for gene: GON7 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GON7 were set to 31481669\nPhenotypes for gene: GON7 were set to Galloway-Mowat syndrome\nReview for gene: GON7 was set to GREEN\nAdded comment: 11 individuals from 5 families. Four of the families had the same homozygous variant, shared haplotype suggestive of founder effect. Clinical features included proteinuria, microcephaly, brain malformations and developmental delay. Supportive functional data. \nSources: Literature",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:03:59.351670+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GON7 as ready",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:03:59.331326+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gon7 has been classified as Green List (High Evidence).",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:03:37.960838+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GON7 as Green List (high evidence)",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:03:37.950844+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gon7 has been classified as Green List (High Evidence).",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T07:02:12.232616+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GON7 was added\ngene: GON7 was added to Proteinuria. Sources: Literature\nMode of inheritance for gene: GON7 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GON7 were set to 31481669\nPhenotypes for gene: GON7 were set to Galloway-Mowat syndrome\nReview for gene: GON7 was set to GREEN\nAdded comment: 11 individuals from 5 families. Four of the families had the same homozygous variant, shared haplotype suggestive of founder effect. Clinical features included proteinuria, microcephaly, brain malformations and developmental delay. Supportive functional data. \nSources: Literature",
"entity_name": "GON7",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:56:52.147340+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAGE3 as ready",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:56:52.137075+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lage3 has been classified as Green List (High Evidence).",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:56:50.060383+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LAGE3 were changed from to Galloway-Mowat syndrome 2, X-linked, MIM# 301006",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:56:23.410927+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAGE3 were set to ",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:55:58.061728+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LAGE3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:55:33.945954+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LAGE3: Rating: GREEN; Mode of pathogenicity: None; Publications: 28805828; Phenotypes: Galloway-Mowat syndrome 2, X-linked, MIM# 301006; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:54:49.701746+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4055",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAGE3 as ready",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:54:49.691077+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4055",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lage3 has been classified as Green List (High Evidence).",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:54:43.066454+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4055",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LAGE3 were changed from to Galloway-Mowat syndrome 2, X-linked, MIM# 301006",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:54:24.610100+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4054",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAGE3 were set to ",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:54:08.349579+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4053",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LAGE3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:53:48.091972+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4052",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LAGE3: Rating: GREEN; Mode of pathogenicity: None; Publications: 28805828; Phenotypes: Galloway-Mowat syndrome 2, X-linked, MIM# 301006; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:52:46.691437+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAGE3 as ready",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:52:46.681099+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lage3 has been classified as Green List (High Evidence).",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:52:43.523778+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.245",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LAGE3 were changed from to Galloway-Mowat syndrome 2, X-linked, MIM# 301006",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:52:26.266780+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.244",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAGE3 were set to ",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:52:01.330214+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.243",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LAGE3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:51:29.910673+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LAGE3: Rating: GREEN; Mode of pathogenicity: None; Publications: 28805828; Phenotypes: Galloway-Mowat syndrome 2, X-linked, MIM# 301006; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "LAGE3",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:48:15.682916+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4052",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LINGO1 as ready",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:48:15.664317+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4052",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lingo1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:48:09.522148+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4052",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LINGO1 were changed from to Mental retardation, autosomal recessive 64, MIM# 618103",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:47:52.513523+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4051",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LINGO1 were set to ",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:47:36.473293+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4050",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LINGO1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:47:21.666748+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: LINGO1 as Amber List (moderate evidence)",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:47:21.653946+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lingo1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:46:53.100671+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LINGO1: Rating: AMBER; Mode of pathogenicity: None; Publications: 31668702; Phenotypes: Mental retardation, autosomal recessive 64, MIM# 618103; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:45:47.333432+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LINGO1 as ready",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:45:47.323596+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lingo1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:45:44.785149+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LINGO1 were changed from to Mental retardation, autosomal recessive 64, MIM# 618103",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:45:19.591975+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.241",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LINGO1 were set to ",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:44:56.213126+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.240",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LINGO1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:44:34.768797+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.239",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: LINGO1 as Amber List (moderate evidence)",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:44:34.757763+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.239",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lingo1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:44:03.240522+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: LINGO1: Changed rating: AMBER",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-09-01T06:43:56.893866+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LINGO1: Rating: ; Mode of pathogenicity: None; Publications: 31668702; Phenotypes: Mental retardation, autosomal recessive 64, MIM# 618103; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LINGO1",
"entity_type": "gene"
},
{
"created": "2020-08-31T23:28:58.170662+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.123",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Marked gene: TRIM8 as ready",
"entity_name": "TRIM8",
"entity_type": "gene"
},
{
"created": "2020-08-31T23:28:58.160359+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.123",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Gene: trim8 has been classified as Green List (High Evidence).",
"entity_name": "TRIM8",
"entity_type": "gene"
},
{
"created": "2020-08-31T23:28:52.681659+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.123",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Classified gene: TRIM8 as Green List (high evidence)",
"entity_name": "TRIM8",
"entity_type": "gene"
},
{
"created": "2020-08-31T23:28:52.673193+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.123",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "Gene: trim8 has been classified as Green List (High Evidence).",
"entity_name": "TRIM8",
"entity_type": "gene"
},
{
"created": "2020-08-31T23:28:04.825352+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.122",
"user_name": "Tiong Tan",
"item_type": "entity",
"text": "gene: TRIM8 was added\ngene: TRIM8 was added to Proteinuria. Sources: Literature\nMode of inheritance for gene: TRIM8 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: TRIM8 were set to 30244534; 32193649\nPhenotypes for gene: TRIM8 were set to intellectual disability; epileptic encephalopathy; nephrotic syndrome; proteinuria\nPenetrance for gene: TRIM8 were set to Complete\nReview for gene: TRIM8 was set to GREEN\nAdded comment: ~50% affected individuals have proteinuria, one confirmed with FSGS \nSources: Literature",
"entity_name": "TRIM8",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:10:00.887535+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OSGEP as ready",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:10:00.878890+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: osgep has been classified as Green List (High Evidence).",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:09:57.129514+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OSGEP were changed from to Galloway-Mowat syndrome 3, MIM# 617729",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:09:38.720065+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OSGEP were set to ",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:09:11.299767+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: OSGEP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:08:46.894142+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: OSGEP: Rating: GREEN; Mode of pathogenicity: None; Publications: 28805828, 28272532; Phenotypes: Galloway-Mowat syndrome 3, MIM# 617729; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:08:37.803412+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OSGEP as ready",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:08:37.795164+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: osgep has been classified as Green List (High Evidence).",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:08:08.407829+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OSGEP as ready",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:08:08.397460+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: osgep has been classified as Green List (High Evidence).",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:08:02.392185+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OSGEP were changed from to Galloway-Mowat syndrome 3, MIM# 617729",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:07:46.597580+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OSGEP were set to ",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:07:29.382462+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4046",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: OSGEP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:07:14.308256+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: OSGEP: Rating: GREEN; Mode of pathogenicity: None; Publications: 28805828, 28272532; Phenotypes: Galloway-Mowat syndrome 3, MIM# 617729; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:06:25.125466+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OSGEP were changed from to Galloway-Mowat syndrome 3, MIM# 617729",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:05:59.340388+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.237",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OSGEP were set to ",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:05:24.358878+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.236",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: OSGEP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T22:04:58.104905+10:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: OSGEP: Rating: GREEN; Mode of pathogenicity: None; Publications: 28805828, 28272532; Phenotypes: Galloway-Mowat syndrome 3, MIM# 617729; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OSGEP",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:59:24.659379+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: NUP107.",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:59:00.634783+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NUP107 as ready",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:59:00.615717+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nup107 has been classified as Green List (High Evidence).",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:58:57.711188+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NUP107 were changed from to Galloway-Mowat syndrome 7, MIM# 618348",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:58:35.797318+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NUP107 were set to ",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:58:09.318086+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NUP107 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:57:48.832316+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: NUP107.",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:57:39.831879+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NUP107: Rating: GREEN; Mode of pathogenicity: None; Publications: 28280135, 28117080, 30179222, 25558065; Phenotypes: Galloway-Mowat syndrome 7, MIM# 618348; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:57:04.853804+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NUP107 as ready",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:57:04.843292+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nup107 has been classified as Green List (High Evidence).",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:56:58.864096+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NUP107 were changed from to Galloway-Mowat syndrome 7, MIM# 618348",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:56:44.382292+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NUP107 were set to ",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:56:29.448895+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4043",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NUP107 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NUP107",
"entity_type": "gene"
},
{
"created": "2020-08-31T21:56:12.187730+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NUP107: Rating: GREEN; Mode of pathogenicity: None; Publications: 28280135, 28117080, 30179222, 25558065; Phenotypes: Galloway-Mowat syndrome 7, MIM# 618348; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NUP107",
"entity_type": "gene"
}
]
}