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{
"count": 220725,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2009",
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"results": [
{
"created": "2020-01-03T19:40:29.724382+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRIM32 as Red List (low evidence)",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:40:29.710741+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:39:48.322664+11:00",
"panel_name": "Bardet Biedl syndrome_VCGS",
"panel_id": 53,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRIM32: Rating: RED; Mode of pathogenicity: None; Publications: 16606853; Phenotypes: Bardet-Biedl syndrome 11, MIM# 615988; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:39:09.259559+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIM32 as ready",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:39:09.245210+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:39:05.784727+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIM32 were changed from to Bardet-Biedl syndrome 11, MIM# 615988",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:38:39.372143+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRIM32 were set to ",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:38:02.779611+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRIM32 as Red List (low evidence)",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:38:02.767046+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:37:09.966385+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRIM32 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:36:44.782704+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRIM32 as Red List (low evidence)",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:36:44.713743+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:36:08.306207+11:00",
"panel_name": "Polydactyly_VCGS",
"panel_id": 159,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRIM32: Rating: RED; Mode of pathogenicity: None; Publications: 16606853; Phenotypes: Bardet-Biedl syndrome 11, MIM# 615988; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:35:22.493010+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRIM32 as ready",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:35:22.480794+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:35:19.224068+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRIM32 were changed from to Bardet-Biedl syndrome 11, MIM# 615988",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:34:53.292851+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRIM32 were set to ",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:34:24.132240+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRIM32 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:33:39.385899+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRIM32 as Red List (low evidence)",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:33:39.371967+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trim32 has been classified as Red List (Low Evidence).",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T19:33:05.123777+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRIM32: Rating: RED; Mode of pathogenicity: None; Publications: 16606853; Phenotypes: Bardet-Biedl syndrome 11, MIM# 615988; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRIM32",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:03:39.983402+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: XPNPEP3 as ready",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:03:39.972250+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:03:33.924006+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1470",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: XPNPEP3 as ready",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:03:33.908457+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1470",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:03:27.127063+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: XPNPEP3 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:02:57.109932+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: XPNPEP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:02:31.804221+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: XPNPEP3 as Red List (low evidence)",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:02:31.742451+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:02:03.160125+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1470",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: XPNPEP3 were changed from to Nephronophthisis-like nephropathy 1, OMIM #613159",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:01:54.474225+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: XPNPEP3 were set to ",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:01:45.641514+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1468",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: XPNPEP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:01:37.850096+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1467",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: XPNPEP3 as Red List (low evidence)",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:01:37.836005+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1467",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:01:26.049195+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: XPNPEP3 were set to ",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:01:25.247066+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1466",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: XPNPEP3: Rating: RED; Mode of pathogenicity: None; Publications: 20179356; Phenotypes: Nephronophthisis-like nephropathy 1, OMIM #613159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:00:53.980839+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.48",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: XPNPEP3 were changed from to Nephronophthisis-like nephropathy 1, OMIM #613159",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:00:32.636947+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.577",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: XPNPEP3 as ready",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:00:32.625582+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.577",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:00:22.524394+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: XPNPEP3 as Red List (low evidence)",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:00:22.508202+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T17:00:14.651963+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.577",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: XPNPEP3 were changed from to Nephronophthisis-like nephropathy 1, OMIM #613159",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:59:50.858330+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: XPNPEP3 as Red List (low evidence)",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:59:50.795626+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:59:20.283786+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.576",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: XPNPEP3 were set to ",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:59:09.151232+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: XPNPEP3: Rating: RED; Mode of pathogenicity: None; Publications: 20179356; Phenotypes: Nephronophthisis-like nephropathy 1, OMIM #613159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:58:26.497708+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: XPNPEP3 as ready",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:58:26.485963+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:58:14.935807+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.575",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: XPNPEP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:58:05.361536+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: XPNPEP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:57:55.318452+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: XPNPEP3 as Red List (low evidence)",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:57:55.303440+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:57:23.644943+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: XPNPEP3 as Red List (low evidence)",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:57:23.633643+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:57:17.052282+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.573",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: XPNPEP3: Rating: RED; Mode of pathogenicity: None; Publications: 20179356; Phenotypes: Nephronophthisis-like nephropathy 1, OMIM #613159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:56:35.817946+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: XPNPEP3 were changed from to Nephronophthisis-like nephropathy 1, OMIM #613159",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:56:09.395203+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: XPNPEP3 were set to ",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:55:46.259347+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: XPNPEP3 as Red List (low evidence)",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:55:46.218315+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpnpep3 has been classified as Red List (Low Evidence).",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:54:49.320430+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: XPNPEP3: Rating: RED; Mode of pathogenicity: None; Publications: 20179356; Phenotypes: Nephronophthisis-like nephropathy 1, OMIM #613159; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "XPNPEP3",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:51:14.674386+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.573",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF423 as ready",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:51:14.662559+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.573",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf423 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:50:46.971895+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF423 as ready",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:50:46.957826+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf423 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:50:46.310120+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.573",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF423 were changed from to Joubert syndrome 19, OMIM# 614844",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:50:33.098933+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF423 were changed from Joubert syndrome 19, OMIM# 614844 to Joubert syndrome 19, OMIM# 614844",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:50:08.835597+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF423 were changed from Joubert syndrome 19, OMIM# 614844 to Joubert syndrome 19, OMIM# 614844",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:49:50.748816+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.572",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZNF423 were set to ",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:49:39.531911+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF423 were changed from to Joubert syndrome 19, OMIM# 614844",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:49:25.114683+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.571",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZNF423 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:48:51.909930+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZNF423 were set to ",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:48:44.933525+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.570",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZNF423 as Red List (low evidence)",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:48:44.920071+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.570",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf423 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:48:19.743393+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZNF423 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:48:11.008026+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.569",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZNF423: Rating: RED; Mode of pathogenicity: None; Publications: 22863007; Phenotypes: Joubert syndrome 19, OMIM# 614844; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:47:15.426898+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF423 as ready",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:47:15.413552+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf423 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:47:14.940956+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.42",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZNF423 as Red List (low evidence)",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:47:14.929061+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.42",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf423 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:46:59.168181+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF423 were changed from to Joubert syndrome 19, OMIM# 614844",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:46:37.742692+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZNF423: Rating: RED; Mode of pathogenicity: None; Publications: 22863007; Phenotypes: Joubert syndrome 19, OMIM# 614844; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:46:25.476657+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZNF423 were set to ",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:45:38.625494+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZNF423 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:45:06.380991+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZNF423 as Red List (low evidence)",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:45:06.366817+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf423 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:44:31.929494+11:00",
"panel_name": "Ciliopathies_VCGS",
"panel_id": 84,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZNF423: Rating: RED; Mode of pathogenicity: None; Publications: 22863007; Phenotypes: Joubert syndrome 19, OMIM# 614844; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ZNF423",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:11:01.436905+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.20",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Classified gene: NPHS2 as Red List (low evidence)",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:11:01.424792+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.20",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Gene: nphs2 has been classified as Red List (Low Evidence).",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:10:34.238576+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.20",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Classified gene: NPHS2 as Red List (low evidence)",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:10:34.170583+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.20",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Gene: nphs2 has been classified as Red List (Low Evidence).",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:10:19.890729+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FN1 as ready",
"entity_name": "FN1",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:10:19.877618+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fn1 has been classified as Green List (High Evidence).",
"entity_name": "FN1",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:10:16.626485+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FN1 as Green List (high evidence)",
"entity_name": "FN1",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:10:16.611565+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fn1 has been classified as Green List (High Evidence).",
"entity_name": "FN1",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:09:58.293165+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.19",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Classified gene: LMX1B as Red List (low evidence)",
"entity_name": "LMX1B",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:09:58.279095+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.19",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Gene: lmx1b has been classified as Red List (Low Evidence).",
"entity_name": "LMX1B",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:09:53.924712+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.19",
"user_name": "chirag patel",
"item_type": "entity",
"text": "reviewed gene: NPHS2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:09:30.782239+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.19",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Classified gene: CUBN as Red List (low evidence)",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:09:30.759598+11:00",
"panel_name": "Haematuria_VCGS_KidGen",
"panel_id": 39,
"panel_version": "0.19",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Gene: cubn has been classified as Red List (Low Evidence).",
"entity_name": "CUBN",
"entity_type": "gene"
},
{
"created": "2020-01-03T16:09:13.531638+11:00",
"panel_name": "Proteinuria_VCGS_KidGen",
"panel_id": 144,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FN1 as Green List (high evidence)",
"entity_name": "FN1",
"entity_type": "gene"
}
]
}