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{
"count": 220818,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=730",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=728",
"results": [
{
"created": "2022-10-06T11:42:24.780690+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.366",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPDU1 as ready",
"entity_name": "MPDU1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:42:24.768405+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.366",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpdu1 has been classified as Red List (Low Evidence).",
"entity_name": "MPDU1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:42:14.040808+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.366",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MPDU1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital disorder of glycosylation, type If, MIM# 609180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MPDU1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:41:54.278852+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.366",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MPDU1 as Red List (low evidence)",
"entity_name": "MPDU1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:41:54.267896+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.366",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpdu1 has been classified as Red List (Low Evidence).",
"entity_name": "MPDU1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:41:18.693931+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.365",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MOCS2 as ready",
"entity_name": "MOCS2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:41:18.685667+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.365",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mocs2 has been classified as Red List (Low Evidence).",
"entity_name": "MOCS2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:41:13.885419+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.365",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MOCS2 were changed from Molybdenum cofactor deficiency to Molybdenum cofactor deficiency B, MIM#252160",
"entity_name": "MOCS2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:40:56.738013+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.364",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MOCS2 as Red List (low evidence)",
"entity_name": "MOCS2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:40:56.728788+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.364",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mocs2 has been classified as Red List (Low Evidence).",
"entity_name": "MOCS2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:40:43.782673+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.363",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MOCS2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Molybdenum cofactor deficiency B MIM#252160; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MOCS2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:39:48.529372+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.346",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: MOCS1.",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:39:21.183469+11:00",
"panel_name": "Miscellaneous Metabolic Disorders",
"panel_id": 3468,
"panel_version": "1.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: MOCS1.",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:39:01.733611+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4959",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: MOCS1.",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:38:44.549051+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1675",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: MOCS1.",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:38:30.548894+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.363",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MOCS1 as ready",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:38:30.538285+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.363",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mocs1 has been classified as Green List (High Evidence).",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:38:24.777766+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.363",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MOCS1 were set to ",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:38:04.340224+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MOCS1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Molybdenum cofactor deficiency A, MIM# 252150; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:37:07.427541+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: MOCS1.",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:36:39.377649+11:00",
"panel_name": "Hyperammonaemia",
"panel_id": 3470,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: MLYCD.",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:36:23.146094+11:00",
"panel_name": "Cardiomyopathy_Paediatric",
"panel_id": 3270,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: MLYCD.",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:36:04.198032+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4959",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: MLYCD.",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:35:28.875782+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.346",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: MLYCD.",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:35:10.683821+11:00",
"panel_name": "Fatty Acid Oxidation Defects",
"panel_id": 103,
"panel_version": "1.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: MLYCD.",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:34:52.985697+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: MLYCD.",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:34:12.848549+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MLYCD as ready",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:34:12.838677+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mlycd has been classified as Green List (High Evidence).",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:34:09.248931+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.362",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MLYCD were changed from Malonyl-CoA decarboxylase deficiency to Malonyl-CoA decarboxylase deficiency, MIM# 248360",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:33:53.704547+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.361",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MLYCD: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Malonyl-CoA decarboxylase deficiency, MIM# 248360; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:33:05.993804+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.361",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZAP70 as ready",
"entity_name": "ZAP70",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:33:05.983802+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.361",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zap70 has been classified as Green List (High Evidence).",
"entity_name": "ZAP70",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:33:02.248672+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.361",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZAP70 were changed from ZAP70-related severe combined immunodeficiency to Immunodeficiency MIM#176947",
"entity_name": "ZAP70",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:32:50.727823+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.360",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZAP70 were set to ",
"entity_name": "ZAP70",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:32:40.283300+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.359",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: ZAP70.",
"entity_name": "ZAP70",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:32:14.928400+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.359",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZEB2 as ready",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:32:14.916904+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.359",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zeb2 has been classified as Red List (Low Evidence).",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:32:09.931325+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.359",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZEB2 were changed from Mowat-Wilson syndrome to Mowat-Wilson syndrome MIM# 235730",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:31:58.815865+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.358",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZEB2 were set to ",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:31:47.997874+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.357",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZEB2 as Red List (low evidence)",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:31:47.988554+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.357",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zeb2 has been classified as Red List (Low Evidence).",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:31:24.274552+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.356",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZIC2 as ready",
"entity_name": "ZIC2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:31:24.265025+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.356",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zic2 has been classified as Red List (Low Evidence).",
"entity_name": "ZIC2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:31:19.922818+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.356",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZIC2 were changed from Holoprosencephaly-5 to Holoprosencephaly MIM#603073",
"entity_name": "ZIC2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:31:04.916010+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.355",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZIC2 were set to ",
"entity_name": "ZIC2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:30:54.388561+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.354",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZIC2 as Red List (low evidence)",
"entity_name": "ZIC2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:30:54.381287+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.354",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zic2 has been classified as Red List (Low Evidence).",
"entity_name": "ZIC2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:30:28.015262+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.353",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZIC3 as ready",
"entity_name": "ZIC3",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:30:28.006315+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.353",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zic3 has been classified as Red List (Low Evidence).",
"entity_name": "ZIC3",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:30:24.527626+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.353",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZIC3 were changed from Heterotaxy to X linked heterotaxy and congenital heart defects MIM:306955",
"entity_name": "ZIC3",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:30:14.304706+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.352",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZIC3 were set to ",
"entity_name": "ZIC3",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:29:59.657694+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.351",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZIC3 as Red List (low evidence)",
"entity_name": "ZIC3",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:29:59.647771+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.351",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zic3 has been classified as Red List (Low Evidence).",
"entity_name": "ZIC3",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:29:11.095890+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZMPSTE24 as ready",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:29:11.087396+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zmpste24 has been classified as Red List (Low Evidence).",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:29:07.479046+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.350",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZMPSTE24 were changed from Restrictive dermopathy to Restrictive dermopathy 1, MIM# MIM:275210",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:28:56.296655+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.349",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZMPSTE24 were set to ",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:28:42.856571+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.348",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZMPSTE24 as Red List (low evidence)",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:28:42.848702+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.348",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zmpste24 has been classified as Red List (Low Evidence).",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:28:21.222842+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.347",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZMPSTE24: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Restrictive dermopathy 1, MIM# MIM:275210; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZMPSTE24",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:27:34.885480+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.347",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF469 as ready",
"entity_name": "ZNF469",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:27:34.876115+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.347",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf469 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF469",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:27:30.647424+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.347",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF469 were changed from Brittle cornea syndrome to Brittle cornea syndrome MIM#229200",
"entity_name": "ZNF469",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:27:17.568549+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.346",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZNF469 were set to ",
"entity_name": "ZNF469",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:27:07.611804+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.345",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZNF469 as Red List (low evidence)",
"entity_name": "ZNF469",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:27:07.602149+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.345",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf469 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF469",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:26:22.551135+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.344",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MLC1 as ready",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:26:22.541378+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.344",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mlc1 has been classified as Red List (Low Evidence).",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:26:18.304707+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.344",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MLC1 were changed from Megalencephalic leukoencephalopathy to Megalencephalic leukoencephalopathy with subcortical cysts OMIM#604004",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:26:04.977295+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.343",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MLC1 as Red List (low evidence)",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:26:04.969424+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.343",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mlc1 has been classified as Red List (Low Evidence).",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:25:53.349661+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MLC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Megalencephalic leukoencephalopathy with subcortical cysts OMIM#604004; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:25:16.727093+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NANS as ready",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:25:16.717880+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nans has been classified as Green List (High Evidence).",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:25:11.678739+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NANS as Green List (high evidence)",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:25:11.667537+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nans has been classified as Green List (High Evidence).",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:24:26.043012+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NBAS as ready",
"entity_name": "NBAS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:24:26.032140+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nbas has been classified as Green List (High Evidence).",
"entity_name": "NBAS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:24:21.992405+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NBAS as Green List (high evidence)",
"entity_name": "NBAS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:24:21.982808+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nbas has been classified as Green List (High Evidence).",
"entity_name": "NBAS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:23:35.163038+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NPR2 as ready",
"entity_name": "NPR2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:23:35.155062+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: npr2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NPR2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:23:30.824740+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NPR2 as Amber List (moderate evidence)",
"entity_name": "NPR2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:23:30.816557+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: npr2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NPR2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:22:58.954079+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NPR2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Acromesomelic dysplasia 1, Maroteaux type - MIM#602875; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NPR2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:21:44.225467+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NPR2 as Green List (high evidence)",
"entity_name": "NPR2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:21:44.217545+11:00",
"panel_name": "Skeletal Dysplasia_Fetal",
"panel_id": 28,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: npr2 has been classified as Green List (High Evidence).",
"entity_name": "NPR2",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:20:57.647223+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MKS1 as ready",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:20:57.638886+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mks1 has been classified as Red List (Low Evidence).",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:20:53.717535+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MKS1 were changed from Meckel syndrome to Joubert syndrome 28, MIM# 617121 MONDO:0014928; Meckel syndrome 1, MIM# 249000 MONDO:0009571; Bardet-Biedl syndrome 13, MIM# 615990 MONDO:0014441",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:20:42.359300+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.341",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MKS1 as Red List (low evidence)",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:20:42.350868+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.341",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mks1 has been classified as Red List (Low Evidence).",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:20:31.445732+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.340",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MKS1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Joubert syndrome 28, MIM# 617121 MONDO:0014928, Meckel syndrome 1, MIM# 249000 MONDO:0009571, Bardet-Biedl syndrome 13, MIM# 615990 MONDO:0014441; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:19:36.124424+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.340",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MKKS as ready",
"entity_name": "MKKS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:19:36.115450+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.340",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mkks has been classified as Red List (Low Evidence).",
"entity_name": "MKKS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:19:31.870341+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.340",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MKKS were changed from Bardet-Biedl syndrome to Bardet-Biedl syndrome 6 (MIM#605231); McKusick-Kaufman syndrome, MIM# 236700",
"entity_name": "MKKS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:19:20.362956+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.339",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MKKS as Red List (low evidence)",
"entity_name": "MKKS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:19:20.354113+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.339",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mkks has been classified as Red List (Low Evidence).",
"entity_name": "MKKS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:19:09.137016+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.338",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MKKS: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Bardet-Biedl syndrome 6 (MIM#605231), McKusick-Kaufman syndrome, MIM# 236700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MKKS",
"entity_type": "gene"
},
{
"created": "2022-10-06T11:17:45.420138+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.338",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAMB3 as ready",
"entity_name": "LAMB3",
"entity_type": "gene"
}
]
}