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{
"count": 221303,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=676",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=674",
"results": [
{
"created": "2022-12-06T20:45:15.193785+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC13A5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Developmental and epileptic encephalopathy 25, with amelogenesis imperfecta MIM#615905; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC13A5",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:42:49.489132+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: SLC25A38.\nTag haematological tag was added to gene: SLC25A38.",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:42:20.659713+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag metabolic tag was added to gene: SLC25A20.",
"entity_name": "SLC25A20",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:41:39.815085+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFRSF11A as ready",
"entity_name": "TNFRSF11A",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:41:39.803398+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf11a has been classified as Green List (High Evidence).",
"entity_name": "TNFRSF11A",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:41:32.745952+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFRSF11A were set to ",
"entity_name": "TNFRSF11A",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:41:15.566338+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: TNFRSF11A.\nTag skeletal tag was added to gene: TNFRSF11A.",
"entity_name": "TNFRSF11A",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:40:42.373871+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFRSF11B as ready",
"entity_name": "TNFRSF11B",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:40:42.360742+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf11b has been classified as Amber List (Moderate Evidence).",
"entity_name": "TNFRSF11B",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:40:33.374053+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFRSF11B were changed from Paget disease to Paget disease of bone 5, juvenile-onset MIM#239000",
"entity_name": "TNFRSF11B",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:39:19.507269+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFRSF11B were set to ",
"entity_name": "TNFRSF11B",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:38:55.768592+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNFRSF11B as Amber List (moderate evidence)",
"entity_name": "TNFRSF11B",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:38:55.751195+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfrsf11b has been classified as Amber List (Moderate Evidence).",
"entity_name": "TNFRSF11B",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:38:43.793365+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: TNFRSF11B.\nTag skeletal tag was added to gene: TNFRSF11B.",
"entity_name": "TNFRSF11B",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:37:51.174492+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFSF11 as ready",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:37:51.160807+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfsf11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:37:47.588150+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFSF11 were changed from Osteopetrosis, autosomal recessive 2 to Osteopetrosis, autosomal recessive 2 MIM#259710",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:37:33.941270+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFSF11 were set to ",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:37:06.961161+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNFSF11 as Amber List (moderate evidence)",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:37:06.949808+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfsf11 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:36:56.063017+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: TNFSF11.\nTag skeletal tag was added to gene: TNFSF11.",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2022-12-06T20:36:38.628536+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNFSF11: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Osteopetrosis, autosomal recessive 2 MIM#259710; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNFSF11",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:27:49.159053+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNNI2 as ready",
"entity_name": "TNNI2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:27:49.146790+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnni2 has been classified as Red List (Low Evidence).",
"entity_name": "TNNI2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:27:45.813305+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNNI2 were changed from Distal arthrogryposis syndrome 2b to Arthrogryposis, distal, type 2B1 MIM#601680",
"entity_name": "TNNI2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:27:34.282437+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNNI2 were set to ",
"entity_name": "TNNI2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:27:23.976505+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNNI2 as Red List (low evidence)",
"entity_name": "TNNI2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:27:23.962745+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnni2 has been classified as Red List (Low Evidence).",
"entity_name": "TNNI2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:26:49.788654+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNNT1 as ready",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:26:49.774254+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnnt1 has been classified as Red List (Low Evidence).",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:26:46.000888+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNNT1 were changed from Nemaline myopathy, Amish type to Nemaline myopathy 5, Amish type MIM#605355",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:26:34.442775+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNNT1 were set to ",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:26:19.219457+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNNT1 as Red List (low evidence)",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:26:19.189551+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnnt1 has been classified as Red List (Low Evidence).",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:26:05.770233+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNNT1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Nemaline myopathy 5, Amish type MIM#605355; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:25:27.096114+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ELP2 as ready",
"entity_name": "ELP2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:25:27.075707+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: elp2 has been classified as Green List (High Evidence).",
"entity_name": "ELP2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:25:22.271538+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ELP2 were changed from to intellectual disability, autosomal recessive 58 MONDO:0014996",
"entity_name": "ELP2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:24:46.957259+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ELP2 were set to ",
"entity_name": "ELP2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:24:11.654227+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ELP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ELP2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:23:03.702451+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ELP2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: intellectual disability, autosomal recessive 58 MONDO:0014996; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ELP2",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:22:00.364297+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AMER1 as ready",
"entity_name": "AMER1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:22:00.351193+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: amer1 has been classified as Green List (High Evidence).",
"entity_name": "AMER1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:21:55.114186+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AMER1 were changed from to Osteopathia striata with cranial sclerosis, OMIM:300373",
"entity_name": "AMER1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:21:20.936962+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: AMER1 were set to ",
"entity_name": "AMER1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:19:21.041890+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AMER1 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "AMER1",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:18:05.091834+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLD as ready",
"entity_name": "DLD",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:18:05.077865+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dld has been classified as Green List (High Evidence).",
"entity_name": "DLD",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:16:12.593483+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DLD were changed from to Dihydrolipoamide dehydrogenase deficiency MIM#246900",
"entity_name": "DLD",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:14:46.474319+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DLD were set to ",
"entity_name": "DLD",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:14:04.117219+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DLD was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DLD",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:13:24.161584+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DLD: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Dihydrolipoamide dehydrogenase deficiency MIM#246900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DLD",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:11:06.390709+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DHCR24 as ready",
"entity_name": "DHCR24",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:11:06.377917+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dhcr24 has been classified as Green List (High Evidence).",
"entity_name": "DHCR24",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:11:02.456037+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DHCR24 were changed from to Desmosterolosis, MIM# 602398",
"entity_name": "DHCR24",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:10:26.569812+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DHCR24 were set to ",
"entity_name": "DHCR24",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:09:44.863384+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DHCR24 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DHCR24",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:08:50.107094+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DOCK8 as ready",
"entity_name": "DOCK8",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:08:50.093350+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dock8 has been classified as Red List (Low Evidence).",
"entity_name": "DOCK8",
"entity_type": "gene"
},
{
"created": "2022-12-06T19:08:45.001575+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DOCK8 were changed from to intellectual developmental disorder, autosomal dominant 2, MIM#614113",
"entity_name": "DOCK8",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:59:56.911028+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5107",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DOCK8 were set to ",
"entity_name": "DOCK8",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:59:17.335976+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DOCK8 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DOCK8",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:57:56.857638+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CDC42 as ready",
"entity_name": "CDC42",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:57:56.845554+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdc42 has been classified as Green List (High Evidence).",
"entity_name": "CDC42",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:56:11.539941+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CDC42 were set to ",
"entity_name": "CDC42",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:55:35.293181+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CDC42 were changed from to Takenouchi-Kosaki syndrome, MIM#616737",
"entity_name": "CDC42",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:54:59.163442+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5103",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CDC42 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CDC42",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:53:55.150094+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALMS1 as ready",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:53:55.136418+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alms1 has been classified as Green List (High Evidence).",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:53:48.158196+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ALMS1 were changed from to Alstrom syndrome, MIM# 203800",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:53:12.568561+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ALMS1 were set to ",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:52:33.359126+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ALMS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:51:57.196073+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5099",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ALMS1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Alstrom syndrome, MIM# 203800; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALMS1",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:46:37.191447+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5099",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BLM as ready",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:46:37.175015+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5099",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: blm has been classified as Red List (Low Evidence).",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:46:32.584509+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5099",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BLM were changed from to Bloom syndrome, MIM# 210900",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:45:42.708062+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5098",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BLM was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:43:46.232615+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5097",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BLM as Red List (low evidence)",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:43:46.219745+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5097",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: blm has been classified as Red List (Low Evidence).",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:37:30.387968+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNNT3 as ready",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:37:30.374075+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnnt3 has been classified as Red List (Low Evidence).",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:37:22.969082+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNNT3 were changed from Arthyrgryposis, distal to Arthrogryposis, distal MIM#618435",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:37:02.090638+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNNT3 were set to ",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:36:49.845639+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNNT3 as Red List (low evidence)",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:36:49.833978+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnnt3 has been classified as Red List (Low Evidence).",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:36:22.381667+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TP53 as ready",
"entity_name": "TP53",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:36:22.367057+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tp53 has been classified as Green List (High Evidence).",
"entity_name": "TP53",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:36:17.345569+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TP53 were changed from Li-Fraumeni syndrome to Li-Fraumeni syndrome MIM#151623",
"entity_name": "TP53",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:36:05.573917+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1173",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TP53 were set to ",
"entity_name": "TP53",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:35:53.326557+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: TP53.\nTag cancer tag was added to gene: TP53.\nTag treatable tag was added to gene: TP53.",
"entity_name": "TP53",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:35:18.238910+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TPM2 as ready",
"entity_name": "TPM2",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:35:18.223750+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tpm2 has been classified as Red List (Low Evidence).",
"entity_name": "TPM2",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:35:14.472337+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TPM2 were changed from Nemaline myopathy; Arthrogryposis multiplex congenita, distal to Arthrgryposis MIM#108120; Nemaline myopathy MIM#609285",
"entity_name": "TPM2",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:35:01.018420+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TPM2 were set to ",
"entity_name": "TPM2",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:34:48.682124+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TPM2 as Red List (low evidence)",
"entity_name": "TPM2",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:34:48.669797+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tpm2 has been classified as Red List (Low Evidence).",
"entity_name": "TPM2",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:32:00.525308+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5096",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: B3GLCT as ready",
"entity_name": "B3GLCT",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:32:00.511729+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5096",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b3glct has been classified as Green List (High Evidence).",
"entity_name": "B3GLCT",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:31:54.041286+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5096",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: B3GLCT were changed from to Peters Plus Syndrome (MIM 261540); Peters anomaly; Growth retardation; Brachydactyly; ID",
"entity_name": "B3GLCT",
"entity_type": "gene"
},
{
"created": "2022-12-06T18:23:58.906004+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5095",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: B3GLCT were set to ",
"entity_name": "B3GLCT",
"entity_type": "gene"
}
]
}