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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2083",
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"results": [
{
"created": "2019-11-28T16:46:16.517575+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FGFR3 as Green List (high evidence)",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:46:16.510075+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgfr3 has been classified as Green List (High Evidence).",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:45:39.784842+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FGFR3 was added\ngene: FGFR3 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert list\nMode of inheritance for gene: FGFR3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: FGFR3 were set to LADD syndrome, MIM#149730\nReview for gene: FGFR3 was set to GREEN\nAdded comment: CAKUT is a feature of LADD syndrome. \nSources: Expert list",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:29:03.944081+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DACT1 as ready",
"entity_name": "DACT1",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:29:03.935744+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dact1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DACT1",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:28:54.760255+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DACT1 as Amber List (moderate evidence)",
"entity_name": "DACT1",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:28:54.753223+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dact1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DACT1",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:28:25.214310+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DACT1 was added\ngene: DACT1 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert list\nMode of inheritance for gene: DACT1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: DACT1 were set to 28054444\nPhenotypes for gene: DACT1 were set to Townes-Brocks syndrome 2, MIM#617466\nReview for gene: DACT1 was set to AMBER\nAdded comment: Single multigenerational family with a heterozygous variant in this gene and features of TBS including CAKUT. \nSources: Expert list",
"entity_name": "DACT1",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:21:37.753007+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COQ7 as ready",
"entity_name": "COQ7",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:21:37.745418+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: coq7 has been classified as Green List (High Evidence).",
"entity_name": "COQ7",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:21:33.292882+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: COQ7 as Green List (high evidence)",
"entity_name": "COQ7",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:21:33.284949+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: coq7 has been classified as Green List (High Evidence).",
"entity_name": "COQ7",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:21:05.090879+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COQ7 was added\ngene: COQ7 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert list\nMode of inheritance for gene: COQ7 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: COQ7 were set to 31240163; 28409910; 26084283\nPhenotypes for gene: COQ7 were set to Coenzyme Q10 deficiency, primary, 8, MIM#616733\nReview for gene: COQ7 was set to GREEN\nAdded comment: Three individuals described in the literature, renal disease prominent in at least two. \nSources: Expert list",
"entity_name": "COQ7",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:13:58.377725+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CENPF as ready",
"entity_name": "CENPF",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:13:58.370799+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cenpf has been classified as Green List (High Evidence).",
"entity_name": "CENPF",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:13:53.981945+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CENPF as Green List (high evidence)",
"entity_name": "CENPF",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:13:53.973411+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cenpf has been classified as Green List (High Evidence).",
"entity_name": "CENPF",
"entity_type": "gene"
},
{
"created": "2019-11-28T16:13:27.102981+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CENPF was added\ngene: CENPF was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert list\nMode of inheritance for gene: CENPF was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CENPF were set to Stromme syndrome, MIM#243605\nReview for gene: CENPF was set to GREEN\nAdded comment: CAKUT is part of the phenotype. \nSources: Expert list",
"entity_name": "CENPF",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:19:51.437658+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EZH2 as ready",
"entity_name": "EZH2",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:19:51.429870+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ezh2 has been classified as Red List (Low Evidence).",
"entity_name": "EZH2",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:19:48.402376+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EZH2 as Red List (low evidence)",
"entity_name": "EZH2",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:19:48.394206+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ezh2 has been classified as Red List (Low Evidence).",
"entity_name": "EZH2",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:19:16.105223+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FOXC1 as ready",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:19:16.097653+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: foxc1 has been classified as Red List (Low Evidence).",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:19:08.488987+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FOXC1 as Red List (low evidence)",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:19:08.480906+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: foxc1 has been classified as Red List (Low Evidence).",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:18:31.423745+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SEMA3A as ready",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:18:31.416603+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sema3a has been classified as Red List (Low Evidence).",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:18:26.831016+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SEMA3A as Red List (low evidence)",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:18:26.821003+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sema3a has been classified as Red List (Low Evidence).",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:18:10.426745+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SEMA3A as Red List (low evidence)",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:18:10.406595+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sema3a has been classified as Red List (Low Evidence).",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:17:53.336596+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SEMA3A as Red List (low evidence)",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:17:53.318651+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sema3a has been classified as Red List (Low Evidence).",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:17:36.944872+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SEMA3A as Red List (low evidence)",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2019-11-28T14:17:36.859202+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sema3a has been classified as Red List (Low Evidence).",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:48:23.421139+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Marked gene: ABCC6 as ready",
"entity_name": "ABCC6",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:48:23.417946+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Agree not an ID gene",
"entity_name": "ABCC6",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:48:23.377007+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: abcc6 has been classified as Red List (Low Evidence).",
"entity_name": "ABCC6",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:47:44.395668+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.18",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Mode of inheritance for gene: ABCC6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ABCC6",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:47:10.299001+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.17",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: ABCC6 as Red List (low evidence)",
"entity_name": "ABCC6",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:47:10.288253+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.17",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: abcc6 has been classified as Red List (Low Evidence).",
"entity_name": "ABCC6",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:45:27.990469+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHD3 as ready",
"entity_name": "CHD3",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:45:27.983379+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chd3 has been classified as Green List (High Evidence).",
"entity_name": "CHD3",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:45:19.766476+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CHD3 as Green List (high evidence)",
"entity_name": "CHD3",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:45:19.758032+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chd3 has been classified as Green List (High Evidence).",
"entity_name": "CHD3",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:43:40.576656+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ABAT as ready",
"entity_name": "ABAT",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:43:40.568537+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: abat has been classified as Green List (High Evidence).",
"entity_name": "ABAT",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:43:36.662538+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ABAT were changed from to GABA-transaminase deficiency, MIM#613163",
"entity_name": "ABAT",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:43:19.786860+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ABAT were set to ",
"entity_name": "ABAT",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:43:03.085822+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ABAT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ABAT",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:41:59.549021+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AAAS as ready",
"entity_name": "AAAS",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:41:59.538448+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aaas has been classified as Green List (High Evidence).",
"entity_name": "AAAS",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:41:55.842540+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AAAS were changed from to Achalasia-addisonianism-alacrimia syndrome, MIM#231550",
"entity_name": "AAAS",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:41:37.179014+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AAAS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AAAS",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:37:20.130955+11:00",
"panel_name": "Renal hypertension and disorders of aldosterone metabolism_KidGen_VCGS",
"panel_id": 190,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Renal hypertension and disorders of aldosterone metabolism_KidGen to Renal hypertension and disorders of aldosterone metabolism_KidGen_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-28T13:24:55.240800+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.8",
"user_name": "San Lin",
"item_type": "panel",
"text": "removed gene:DNAJB11 from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-28T13:24:44.514297+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.7",
"user_name": "San Lin",
"item_type": "panel",
"text": "removed gene:DZIP1L from the panel",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-28T13:11:12.354067+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AHI1 as ready",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:11:12.346658+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ahi1 has been classified as Green List (High Evidence).",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:11:08.201118+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AHI1 were changed from Joubert syndrome 3 to Joubert syndrome 3, MIM#608629",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:10:31.088950+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AHI1 as Green List (high evidence)",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2019-11-28T13:10:31.080530+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ahi1 has been classified as Green List (High Evidence).",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:40:58.747329+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.0",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: SEMA3A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "SEMA3A",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:40:25.209514+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.0",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: FOXC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:39:46.146052+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS",
"panel_id": 63,
"panel_version": "0.0",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: EZH2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "EZH2",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:24:56.907404+11:00",
"panel_name": "Renal amyloidosis_KidGen_VCGS",
"panel_id": 191,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Amyloidosis_KidGen_VCGS to Renal amyloidosis_KidGen_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-28T10:23:19.946482+11:00",
"panel_name": "Amyloidosis_KidGen_VCGS",
"panel_id": 191,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel name changed from Amyloidosis_KidGen to Amyloidosis_KidGen_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-28T10:22:08.933298+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NLRP3 as ready",
"entity_name": "NLRP3",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:22:08.925993+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nlrp3 has been classified as Green List (High Evidence).",
"entity_name": "NLRP3",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:22:05.823305+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NLRP3 were changed from Muckle-Wells syndrome to Muckle-Wells syndrome, MIM#191900",
"entity_name": "NLRP3",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:21:51.142354+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NLRP3 as Green List (high evidence)",
"entity_name": "NLRP3",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:21:51.134968+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nlrp3 has been classified as Green List (High Evidence).",
"entity_name": "NLRP3",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:20:58.638809+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LYZ as ready",
"entity_name": "LYZ",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:20:58.630948+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lyz has been classified as Green List (High Evidence).",
"entity_name": "LYZ",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:20:55.507048+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LYZ were changed from Amyloidosis, renal to Amyloidosis, renal, MIM#105200",
"entity_name": "LYZ",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:20:44.326347+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: LYZ as Green List (high evidence)",
"entity_name": "LYZ",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:20:44.319107+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lyz has been classified as Green List (High Evidence).",
"entity_name": "LYZ",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:20:15.237473+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GSN as ready",
"entity_name": "GSN",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:20:15.230077+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gsn has been classified as Green List (High Evidence).",
"entity_name": "GSN",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:20:11.442613+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GSN were changed from Amyloidosis, Finnish type to Amyloidosis, Finnish type, MIM#105200",
"entity_name": "GSN",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:19:58.584250+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GSN as Green List (high evidence)",
"entity_name": "GSN",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:19:58.576427+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gsn has been classified as Green List (High Evidence).",
"entity_name": "GSN",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:19:16.068555+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGA as ready",
"entity_name": "FGA",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:19:16.061339+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fga has been classified as Green List (High Evidence).",
"entity_name": "FGA",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:19:13.165582+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FGA were changed from Amyloidosis, familial visceral to Amyloidosis, familial visceral, MIM#105200",
"entity_name": "FGA",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:18:56.440149+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FGA as Green List (high evidence)",
"entity_name": "FGA",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:18:56.432501+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fga has been classified as Green List (High Evidence).",
"entity_name": "FGA",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:18:12.768317+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: APOA1 as ready",
"entity_name": "APOA1",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:18:12.760334+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: apoa1 has been classified as Green List (High Evidence).",
"entity_name": "APOA1",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:18:09.909169+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: APOA1 were changed from Amyloidosis, 3 or more types to Amyloidosis, 3 or more types, MIM#105200",
"entity_name": "APOA1",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:17:55.630231+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: APOA1 as Green List (high evidence)",
"entity_name": "APOA1",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:17:55.622762+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: apoa1 has been classified as Green List (High Evidence).",
"entity_name": "APOA1",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:17:44.256519+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.3",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: FAN1 was added\ngene: FAN1 was added to Renal ciliopathies and nephronophthisis_KidGen. Sources: Expert list\nMode of inheritance for gene: FAN1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FAN1 were set to PubMed: 22772369; 16678356; 7847351; 8546134\nPhenotypes for gene: FAN1 were set to Interstitial nephritis, karyomegalic\nReview for gene: FAN1 was set to GREEN\nAdded comment: Sources: Expert list",
"entity_name": "FAN1",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:15:06.798151+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.1",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "gene: AHI1 was added\ngene: AHI1 was added to Renal ciliopathies and nephronophthisis_KidGen. Sources: Expert list\nMode of inheritance for gene: AHI1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AHI1 were set to PubMed: 15322546; 15467982; 16453322; 29146704\nPhenotypes for gene: AHI1 were set to Joubert syndrome 3\nReview for gene: AHI1 was set to GREEN\nAdded comment: Sources: Expert list",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:12:57.259849+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.0",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: DZIP1L: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "DZIP1L",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:12:43.249631+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen",
"panel_id": 193,
"panel_version": "0.0",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: DNAJB11: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "DNAJB11",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:01:04.413294+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.7",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Publications for gene GSN were changed from PubMed: 8395367; 2176164; 8684801; 6975851; 29167514 to PubMed: 8395367; 2176164; 8684801; 6975851; 29167514",
"entity_name": "GSN",
"entity_type": "gene"
},
{
"created": "2019-11-28T10:00:55.659360+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.6",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: GSN: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 8395367, 2176164, 8684801, 6975851, 29167514; Phenotypes: Amyloidosis, Finnish type; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GSN",
"entity_type": "gene"
},
{
"created": "2019-11-28T09:59:58.875578+11:00",
"panel_name": "Amyloidosis_KidGen",
"panel_id": 191,
"panel_version": "0.6",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Source KidGen_Amyloidosis v38.1.0 was removed from GSN.\nSource Expert list was added to GSN.\nMode of inheritance for gene GSN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: GSN were changed from to Amyloidosis, Finnish type\nPublications for gene GSN were changed from PubMed: 8395367; 2176164; 8684801; 6975851 to PubMed: 8395367; 2176164; 8684801; 6975851",
"entity_name": "GSN",
"entity_type": "gene"
}
]
}