HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 221415,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=361",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=359",
"results": [
{
"created": "2024-10-24T13:53:17.294213+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.384",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rtn4ip1 has been classified as Red List (Low Evidence).",
"entity_name": "RTN4IP1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:52:20.027305+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.383",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RNU7-1 as ready",
"entity_name": "RNU7-1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:52:20.013418+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.383",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnu7-1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "RNU7-1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:52:14.465483+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.383",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RNU7-1 as Amber List (moderate evidence)",
"entity_name": "RNU7-1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:52:14.451750+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.383",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rnu7-1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "RNU7-1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:50:28.162879+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.382",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PUM1 as ready",
"entity_name": "PUM1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:50:28.150779+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.382",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pum1 has been classified as Red List (Low Evidence).",
"entity_name": "PUM1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:50:23.821947+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.382",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PUM1 as Red List (low evidence)",
"entity_name": "PUM1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:50:23.797995+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.382",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pum1 has been classified as Red List (Low Evidence).",
"entity_name": "PUM1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:49:36.393653+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.381",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGAP2 as ready",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:49:36.377726+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.381",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgap2 has been classified as Red List (Low Evidence).",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:45:40.811318+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.381",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PGAP2 as Red List (low evidence)",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:45:40.800651+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.381",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgap2 has been classified as Red List (Low Evidence).",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:44:53.774961+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.380",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF5C as ready",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:44:53.762213+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.380",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif5c has been classified as Red List (Low Evidence).",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:44:46.960537+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.380",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KIF5C as Red List (low evidence)",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:44:46.951214+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.380",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif5c has been classified as Red List (Low Evidence).",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:44:03.996076+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCNK9 as ready",
"entity_name": "KCNK9",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:44:03.982426+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnk9 has been classified as Red List (Low Evidence).",
"entity_name": "KCNK9",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:43:51.078542+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KCNK9 as Red List (low evidence)",
"entity_name": "KCNK9",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:43:51.060802+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.379",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnk9 has been classified as Red List (Low Evidence).",
"entity_name": "KCNK9",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:43:07.852757+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.378",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IREB2 as ready",
"entity_name": "IREB2",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:43:07.838082+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.378",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ireb2 has been classified as Red List (Low Evidence).",
"entity_name": "IREB2",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:42:59.852081+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.378",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IREB2 as Red List (low evidence)",
"entity_name": "IREB2",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:42:59.813936+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.378",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ireb2 has been classified as Red List (Low Evidence).",
"entity_name": "IREB2",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:42:17.295983+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.377",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EBF3 as ready",
"entity_name": "EBF3",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:42:17.283377+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.377",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ebf3 has been classified as Red List (Low Evidence).",
"entity_name": "EBF3",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:42:08.901635+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.377",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EBF3 as Red List (low evidence)",
"entity_name": "EBF3",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:42:08.880935+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.377",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ebf3 has been classified as Red List (Low Evidence).",
"entity_name": "EBF3",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:41:22.809330+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.376",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COQ4 as ready",
"entity_name": "COQ4",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:41:22.798747+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.376",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: coq4 has been classified as Red List (Low Evidence).",
"entity_name": "COQ4",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:41:15.746868+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.376",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: COQ4 as Red List (low evidence)",
"entity_name": "COQ4",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:41:15.730893+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.376",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: coq4 has been classified as Red List (Low Evidence).",
"entity_name": "COQ4",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:40:29.202419+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.375",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLN6 as ready",
"entity_name": "CLN6",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:40:29.175524+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.375",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cln6 has been classified as Red List (Low Evidence).",
"entity_name": "CLN6",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:40:18.494004+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.375",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CLN6 as Red List (low evidence)",
"entity_name": "CLN6",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:40:18.477176+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.375",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cln6 has been classified as Red List (Low Evidence).",
"entity_name": "CLN6",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:06:24.961418+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.374",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BRAF as Amber List (moderate evidence)",
"entity_name": "BRAF",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:06:24.943576+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.374",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: braf has been classified as Amber List (Moderate Evidence).",
"entity_name": "BRAF",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:06:16.148964+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.373",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BRAF as ready",
"entity_name": "BRAF",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:06:16.114753+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.373",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: braf has been classified as Amber List (Moderate Evidence).",
"entity_name": "BRAF",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:04:26.376863+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.373",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BRAF as Amber List (moderate evidence)",
"entity_name": "BRAF",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:04:26.339816+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.373",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: braf has been classified as Amber List (Moderate Evidence).",
"entity_name": "BRAF",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:01:14.078119+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALDH7A1 as ready",
"entity_name": "ALDH7A1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:01:14.049038+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aldh7a1 has been classified as Red List (Low Evidence).",
"entity_name": "ALDH7A1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:01:08.911044+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ALDH7A1 as Red List (low evidence)",
"entity_name": "ALDH7A1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:01:08.890140+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aldh7a1 has been classified as Red List (Low Evidence).",
"entity_name": "ALDH7A1",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:00:00.150994+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PIK3CA as Red List (low evidence)",
"entity_name": "PIK3CA",
"entity_type": "gene"
},
{
"created": "2024-10-24T13:00:00.134263+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pik3ca has been classified as Red List (Low Evidence).",
"entity_name": "PIK3CA",
"entity_type": "gene"
},
{
"created": "2024-10-24T12:59:36.349452+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIK3CA as ready",
"entity_name": "PIK3CA",
"entity_type": "gene"
},
{
"created": "2024-10-24T12:59:36.329402+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pik3ca has been classified as Red List (Low Evidence).",
"entity_name": "PIK3CA",
"entity_type": "gene"
},
{
"created": "2024-10-24T12:59:28.349058+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PIK3CA as Red List (low evidence)",
"entity_name": "PIK3CA",
"entity_type": "gene"
},
{
"created": "2024-10-24T12:59:28.323665+11:00",
"panel_name": "Cerebral Palsy",
"panel_id": 73,
"panel_version": "1.371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pik3ca has been classified as Red List (Low Evidence).",
"entity_name": "PIK3CA",
"entity_type": "gene"
},
{
"created": "2024-10-24T10:37:58.531712+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.471",
"user_name": "Michelle Torres",
"item_type": "entity",
"text": "reviewed gene: ADAMTSL2: Rating: GREEN; Mode of pathogenicity: None; Publications: 20301776, 38300707; Phenotypes: Geleophysic dysplasia 1 MIM#231050; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADAMTSL2",
"entity_type": "gene"
},
{
"created": "2024-10-24T09:59:22.858774+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.471",
"user_name": "Michelle Torres",
"item_type": "entity",
"text": "reviewed gene: ADA: Rating: GREEN; Mode of pathogenicity: None; Publications: 20301656, 8673127; Phenotypes: Severe combined immunodeficiency due to ADA deficiency MIM#102700 AR, Smo, Adenosine deaminase deficiency, partial MIM#102700 AR,SMo.; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADA",
"entity_type": "gene"
},
{
"created": "2024-10-23T21:03:18.319463+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAT as ready",
"entity_name": "LAT",
"entity_type": "gene"
},
{
"created": "2024-10-23T21:03:18.305594+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lat has been classified as Green List (High Evidence).",
"entity_name": "LAT",
"entity_type": "gene"
},
{
"created": "2024-10-23T21:03:10.985153+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAT were set to 27522155; 27242165",
"entity_name": "LAT",
"entity_type": "gene"
},
{
"created": "2024-10-23T21:02:53.765699+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.470",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LAT: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Immunodeficiency 52, MIM# 617514, severe combined immunodeficiency due to LAT deficiency MONDO:0044721; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAT",
"entity_type": "gene"
},
{
"created": "2024-10-23T21:00:59.313360+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF5A as ready",
"entity_name": "KIF5A",
"entity_type": "gene"
},
{
"created": "2024-10-23T21:00:59.293526+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif5a has been classified as Amber List (Moderate Evidence).",
"entity_name": "KIF5A",
"entity_type": "gene"
},
{
"created": "2024-10-23T21:00:55.729314+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF5A were changed from Spastic paraplegia 10, autosomal dominant, MIM# 604187; inherited neurodegenerative disorder MONDO:0024237 to Spastic paraplegia 10, autosomal dominant, MIM# 604187; inherited neurodegenerative disorder MONDO:0024237",
"entity_name": "KIF5A",
"entity_type": "gene"
},
{
"created": "2024-10-23T21:00:33.762696+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.2069",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "gene: AJAP1 was added\ngene: AJAP1 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: AJAP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: AJAP1 were set to 38985877\nPhenotypes for gene: AJAP1 were set to neurodevelopmental disorder, MONDO:0700092\nReview for gene: AJAP1 was set to GREEN\nAdded comment: PMID:38985877 reported five unrelated individuals with monoallelic variants or a deletion in AJAP1 gene and they presented with epilepsy, neurodevelopmental problems, or intellectual disability. There is also supporting functional evidence available. \nSources: Literature",
"entity_name": "AJAP1",
"entity_type": "gene"
},
{
"created": "2024-10-23T21:00:11.694863+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6578",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF5A were changed from to Spastic paraplegia 10, autosomal dominant, MIM# 604187; inherited neurodegenerative disorder MONDO:0024237",
"entity_name": "KIF5A",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:59:26.231378+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6577",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF5A were set to 18853458",
"entity_name": "KIF5A",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:58:44.943026+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6576",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF5A were set to ",
"entity_name": "KIF5A",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:57:57.077017+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6575",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF5A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KIF5A",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:57:25.197684+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KIF5A as Amber List (moderate evidence)",
"entity_name": "KIF5A",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:57:25.188387+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif5a has been classified as Amber List (Moderate Evidence).",
"entity_name": "KIF5A",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:56:29.545199+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6573",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KIF5A as Amber List (moderate evidence)",
"entity_name": "KIF5A",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:56:29.523179+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6573",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif5a has been classified as Amber List (Moderate Evidence).",
"entity_name": "KIF5A",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:54:42.346644+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6572",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF7 as ready",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:54:42.336710+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6572",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif7 has been classified as Green List (High Evidence).",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:54:32.838330+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6572",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF7 were changed from acrocallosal syndrome MONDO:0008708; KIF7-related ciliopathy MONDO:0800463; Joubert syndrome 12 MIM#200990 to acrocallosal syndrome MONDO:0008708; KIF7-related ciliopathy MONDO:0800463; Joubert syndrome 12 MIM#200990",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:53:56.566535+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6571",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIF7 were changed from to acrocallosal syndrome MONDO:0008708; KIF7-related ciliopathy MONDO:0800463; Joubert syndrome 12 MIM#200990",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:51:46.575759+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6570",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KIF7 were set to ",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:51:09.461107+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6569",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF7 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:50:26.160799+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6569",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KIF7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KIF7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:46:48.004492+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6568",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KLHL7 as ready",
"entity_name": "KLHL7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:46:47.959067+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6568",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: klhl7 has been classified as Green List (High Evidence).",
"entity_name": "KLHL7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:46:08.373352+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6568",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KLHL7 were changed from to PERCHING syndrome MONDO:0014890; acrocallosal syndrome MONDO:0008708",
"entity_name": "KLHL7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:45:18.785261+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6567",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KLHL7 were set to 27392078; 30142437; 29074562",
"entity_name": "KLHL7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:44:35.434813+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6566",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KLHL7 were set to ",
"entity_name": "KLHL7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:43:32.405972+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6565",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KLHL7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "KLHL7",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:24:43.694323+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6564",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: L2HGDH as ready",
"entity_name": "L2HGDH",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:24:43.676111+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6564",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: l2hgdh has been classified as Green List (High Evidence).",
"entity_name": "L2HGDH",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:24:36.238349+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6564",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: L2HGDH were changed from to L-2-hydroxyglutaric aciduria, MIM#236792",
"entity_name": "L2HGDH",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:23:38.215549+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6563",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: L2HGDH were set to ",
"entity_name": "L2HGDH",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:22:52.449569+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6562",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: L2HGDH was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "L2HGDH",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:22:17.593124+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6561",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: L2HGDH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "L2HGDH",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:21:09.446867+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6560",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAMA1 as ready",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:21:09.434699+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6560",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lama1 has been classified as Green List (High Evidence).",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:20:35.538850+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6560",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LAMA1 were changed from to ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome MONDO:0014419",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:19:54.906940+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAMA1 were set to ",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:19:10.436809+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6558",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LAMA1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:18:27.376699+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6557",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LAMA1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2024-10-23T20:17:43.738830+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6556",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LAMA1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2024-10-23T19:21:16.610215+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6555",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LAMA1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2024-10-23T19:20:19.555771+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6554",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ISPD as ready",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2024-10-23T19:20:19.541391+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.6554",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ispd has been classified as Green List (High Evidence).",
"entity_name": "ISPD",
"entity_type": "gene"
}
]
}