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{
"count": 221272,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1038",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1036",
"results": [
{
"created": "2022-01-20T17:41:38.819380+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TUBG1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:41:09.769665+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VDR as ready",
"entity_name": "VDR",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:41:09.755676+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vdr has been classified as Red List (Low Evidence).",
"entity_name": "VDR",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:41:06.266986+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VDR were changed from RICKETS VITAMIN D-DEPENDENT TYPE 2A to Rickets, vitamin D-resistant, type IIA, MIM#\t277440",
"entity_name": "VDR",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:39:09.981553+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VEGFC were changed from Lymphatic malformation 4 to Lymphatic malformation 4, MIM# 615907",
"entity_name": "VEGFC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:38:57.282036+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2524",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: VEGFC was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "VEGFC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:38:45.423472+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: VEGFC as Amber List (moderate evidence)",
"entity_name": "VEGFC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:38:45.412964+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vegfc has been classified as Amber List (Moderate Evidence).",
"entity_name": "VEGFC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:38:34.436815+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: VEGFC: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Lymphatic malformation 4, MIM# 615907; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "VEGFC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:37:14.802639+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VEGFC as ready",
"entity_name": "VEGFC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:37:14.791116+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vegfc has been classified as Red List (Low Evidence).",
"entity_name": "VEGFC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:36:45.071846+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WNT3 as ready",
"entity_name": "WNT3",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:36:44.997338+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnt3 has been classified as Red List (Low Evidence).",
"entity_name": "WNT3",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:36:41.063054+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WNT3 were changed from TETRA-AMELIA SYNDROME to Tetra-amelia syndrome 1, OMIM #273395",
"entity_name": "WNT3",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:39:22.106634+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2521",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: WNT1 as ready",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:39:22.097976+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2521",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: wnt1 has been classified as Green List (High Evidence).",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:39:01.435425+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2521",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: WNT1 were set to ",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:29:00.133086+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2520",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: WNT5A as ready",
"entity_name": "WNT5A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:29:00.119937+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2520",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: wnt5a has been classified as Green List (High Evidence).",
"entity_name": "WNT5A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:28:55.961601+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2520",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: WNT5A were changed from WNT5A-RELATED ROBINOW SYNDROME, AUTOSOMAL DOMINANT to Robinow syndrome, autosomal dominant 1; OMIM# 180700",
"entity_name": "WNT5A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:28:44.615727+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2519",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: WNT5A were set to ",
"entity_name": "WNT5A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:28:32.637073+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2518",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Mode of inheritance for gene: WNT5A was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WNT5A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:26:09.163585+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2517",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: WNT7A as ready",
"entity_name": "WNT7A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:26:09.152961+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2517",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: wnt7a has been classified as Green List (High Evidence).",
"entity_name": "WNT7A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:25:45.840999+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2517",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: WNT7A were changed from FUHRMANN SYNDROME; LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME to Fuhrmann syndrome, MIM# 228930; Ulna and fibula, absence of, with severe limb deficiency, MIM# 276820",
"entity_name": "WNT7A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:25:32.308021+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10663",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: WNT7A as ready",
"entity_name": "WNT7A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:25:32.293769+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10663",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: wnt7a has been classified as Green List (High Evidence).",
"entity_name": "WNT7A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:25:21.869896+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10663",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: WNT7A were changed from to Fuhrmann syndrome, MIM# 228930; Ulna and fibula, absence of, with severe limb deficiency, MIM# 276820",
"entity_name": "WNT7A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:24:52.469996+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10662",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: WNT7A were set to ",
"entity_name": "WNT7A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:23:49.906093+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10661",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Mode of inheritance for gene: WNT7A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WNT7A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:19:40.668080+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10660",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "reviewed gene: WNT7A: Rating: GREEN; Mode of pathogenicity: None; Publications: 21344627, 20949531, 16826533; Phenotypes: Fuhrmann syndrome, MIM# 228930, Ulna and fibula, absence of, with severe limb deficiency, MIM# 276820; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "WNT7A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:13:34.085602+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2516",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: WNT7A were set to ",
"entity_name": "WNT7A",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:11:44.057830+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.83",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: WT1 as ready",
"entity_name": "WT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:11:44.048313+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.83",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: wt1 has been classified as Green List (High Evidence).",
"entity_name": "WT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:11:40.221128+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.83",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: WT1 were changed from to Denys-Drash syndrome, MIM# 194080; Frasier syndrome, MIM#136680; Wilms tumor, type 1, MIM#194070; Nephrotic syndrome, type 4, MIM#256370",
"entity_name": "WT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:11:13.682623+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.82",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Mode of inheritance for gene: WT1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:10:40.621143+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2515",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: WT1 as ready",
"entity_name": "WT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:10:40.611866+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2515",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: wt1 has been classified as Green List (High Evidence).",
"entity_name": "WT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:10:29.021876+11:00",
"panel_name": "Incidentalome",
"panel_id": 126,
"panel_version": "0.81",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "reviewed gene: WT1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Denys-Drash syndrome, MIM# 194080, Frasier syndrome, MIM#136680, Wilms tumor, type 1, MIM#194070, Nephrotic syndrome, type 4, MIM#256370; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "WT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:07:37.574464+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2515",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: WT1 were changed from DENYS-DRASH SYNDROME; FRASIER SYNDROME FRASIER SYNDROME FRASIER SYNDROME to Denys-Drash syndrome, MIM# 194080; Frasier syndrome, MIM#136680",
"entity_name": "WT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:06:25.435914+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2514",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Mode of inheritance for gene: WT1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:03:07.434431+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2513",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: XRCC4 as ready",
"entity_name": "XRCC4",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:03:07.424042+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2513",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: xrcc4 has been classified as Green List (High Evidence).",
"entity_name": "XRCC4",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:02:51.485644+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2513",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: XRCC4 were changed from PRIMORDIAL DWARFISM to Short stature, microcephaly, and endocrine dysfunction, MIM#616541",
"entity_name": "XRCC4",
"entity_type": "gene"
},
{
"created": "2022-01-20T10:02:27.718857+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2512",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: XRCC4 were set to ",
"entity_name": "XRCC4",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:59:57.759430+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2511",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: XYLT1 as ready",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:59:57.749484+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2511",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: xylt1 has been classified as Green List (High Evidence).",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:59:48.044807+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10660",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: XYLT1 as ready",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:59:48.035813+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10660",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: xylt1 has been classified as Green List (High Evidence).",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:59:42.263066+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2511",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: XYLT1 were changed from DESBUQUOIS DYSPLASIA 2 to Desbuquois dysplasia 2, MIM# 615777; Baratela-Scott syndrome",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:59:34.720311+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10660",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: XYLT1 were set to ",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:58:38.884554+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2510",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: XYLT1 were set to ",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:47:16.542154+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2509",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: ZC4H2 as ready",
"entity_name": "ZC4H2",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:47:16.528095+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2509",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: zc4h2 has been classified as Green List (High Evidence).",
"entity_name": "ZC4H2",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:47:10.411415+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2509",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: ZC4H2 were changed from Wieacker-Wolff syndrome, OMIM:314580; Wieacker-Wolff syndrome, female-restricted, OMIM:301041 to Wieacker-Wolff syndrome, OMIM#314580; Wieacker-Wolff syndrome, female-restricted, OMIM#301041",
"entity_name": "ZC4H2",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:46:42.247219+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2508",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: ZC4H2 were set to 30712880",
"entity_name": "ZC4H2",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:44:50.046094+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2507",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: ZEB2 as ready",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:44:50.036156+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2507",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: zeb2 has been classified as Green List (High Evidence).",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:44:12.877554+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2507",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: ZEB2 were changed from MOWAT-WILSON SYNDROME to Mowat-Wilson syndrome, MIM# 235730; MONDO:0009341",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:43:53.591398+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2506",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: ZEB2 were set to ",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:43:33.531277+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2505",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZEB2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZEB2",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:40:59.122728+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10659",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: ZIC1 were changed from to Structural brain anomalies with impaired intellectual development and craniosynostosis, OMIM#618736",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:40:14.879109+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10658",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: ZIC1 as ready",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:40:14.869429+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10658",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: zic1 has been classified as Green List (High Evidence).",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:40:02.097460+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10658",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: ZIC1 were set to ",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:39:42.099087+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10657",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZIC1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:39:08.624475+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10656",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "reviewed gene: ZIC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26340333, 30391508; Phenotypes: Structural brain anomalies with impaired intellectual development and craniosynostosis, OMIM#618736; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:35:43.266149+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2504",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: ZIC1 as ready",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:35:43.253184+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2504",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: zic1 has been classified as Green List (High Evidence).",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:35:31.555250+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2504",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: ZIC1 were changed from CRANIOSYNOSTOSIS 6 to Structural brain anomalies with impaired intellectual development and craniosynostosis; OMIM#618736",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:35:06.849889+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2503",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: ZIC1 were set to ",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:34:44.147545+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2502",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZIC1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZIC1",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:31:24.299275+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2501",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: ZIC3 as ready",
"entity_name": "ZIC3",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:31:24.289252+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2501",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: zic3 has been classified as Green List (High Evidence).",
"entity_name": "ZIC3",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:28:44.212457+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2501",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: ZIC3 were changed from HETEROTAXY SYNDROME; VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS to Congenital heart defects, nonsyndromic, 1, X-linked, MIM#306955; Heterotaxy, visceral, 1, X-linked, MIM#306955; VACTERL association, X-linked, MIM#314390",
"entity_name": "ZIC3",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:23:13.810742+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2500",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: ZIC3 were set to ",
"entity_name": "ZIC3",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:16:15.760088+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2499",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: ZNF462 as ready",
"entity_name": "ZNF462",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:16:15.749907+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2499",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: znf462 has been classified as Green List (High Evidence).",
"entity_name": "ZNF462",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:16:09.900372+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2499",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF462 were changed from Craniofacial anomalies, corpus callosum dysgenesis, ptosis, and developmental delay to Weiss-Kruszka syndrome; OMIM#618619",
"entity_name": "ZNF462",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:15:39.135957+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2498",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: ZNF462 were set to ",
"entity_name": "ZNF462",
"entity_type": "gene"
},
{
"created": "2022-01-20T09:15:25.705837+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2497",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZNF462 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZNF462",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:58:10.708870+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STIL as ready",
"entity_name": "STIL",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:58:10.698712+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stil has been classified as Green List (High Evidence).",
"entity_name": "STIL",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:58:05.999145+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STIL were set to 29230157",
"entity_name": "STIL",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:57:50.699460+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2495",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: STIL as Green List (high evidence)",
"entity_name": "STIL",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:57:50.669214+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2495",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stil has been classified as Green List (High Evidence).",
"entity_name": "STIL",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:57:36.064695+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: More than 10 unrelated families reported.; to: More than 10 unrelated families reported. Brain abnormalities in one.",
"entity_name": "STIL",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:56:26.800301+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STRADA as ready",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:56:26.791114+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: strada has been classified as Green List (High Evidence).",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:56:16.940643+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STRADA were changed from to Polyhydramnios, megalencephaly, and symptomatic epilepsy, OMIM:611087; Polyhydramnios, megalencephaly, and symptomatic epilepsy, MONDO:0012611",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:55:56.499996+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10655",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STRADA were set to ",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:55:35.943944+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10654",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: STRADA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:55:16.004609+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10653",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: STRADA: Rating: GREEN; Mode of pathogenicity: None; Publications: 17522105, 27170158, 28688840; Phenotypes: Polyhydramnios, megalencephaly, and symptomatic epilepsy, OMIM:611087, Polyhydramnios, megalencephaly, and symptomatic epilepsy, MONDO:0012611; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:54:14.985717+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STRADA as ready",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:54:14.975391+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: strada has been classified as Green List (High Evidence).",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:54:10.725204+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STRADA were set to ",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:53:59.327573+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: STRADA as Green List (high evidence)",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:53:59.316255+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: strada has been classified as Green List (High Evidence).",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:53:21.188186+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2492",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SUFU as ready",
"entity_name": "SUFU",
"entity_type": "gene"
},
{
"created": "2022-01-20T07:53:21.179158+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2492",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sufu has been classified as Green List (High Evidence).",
"entity_name": "SUFU",
"entity_type": "gene"
}
]
}