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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1095",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1093",
"results": [
{
"created": "2021-12-06T18:26:19.035615+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NFIX were set to ",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:25:51.303830+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NFIX was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:25:30.367171+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NFIX: Rating: GREEN; Mode of pathogenicity: None; Publications: 33034087, 29897170, 30548146, 25118028; Phenotypes: Sotos syndrome 2 (MIM#614753), Marshall-Smith syndrome, MIM# 602535; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:24:20.724882+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1054",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NFIX was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:23:45.676447+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1053",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NFIX as ready",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:23:45.660962+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1053",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nfix has been classified as Green List (High Evidence).",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:23:41.101577+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1053",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NFIX were changed from SOTOS-LIKE SYNDROME; MARSHALL-SMITH SYNDROME to Sotos syndrome 2 (MIM#614753); Marshall-Smith syndrome, MIM# 602535",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:23:23.601445+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1052",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NFIX were set to ",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:23:08.631106+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1051",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NFIX: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Marshall-Smith syndrome, MIM# 602535; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NFIX",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:20:46.514511+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1051",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEU1 as ready",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:20:46.500993+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1051",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neu1 has been classified as Green List (High Evidence).",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:20:42.685081+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1051",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEU1 were changed from SIALIDOSIS to Sialidosis, type I, type II (MIM#256550)",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:20:30.640248+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1050",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEU1 were set to ",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:20:03.293190+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GFM1 as ready",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:20:03.281563+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gfm1 has been classified as Green List (High Evidence).",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:19:52.657853+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GFM1 were changed from COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1 to Combined oxidative phosphorylation deficiency 1 MIM#609060",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:19:39.220429+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GFM1 were set to ",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:19:11.928687+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GFM1 as ready",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:19:11.918507+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gfm1 has been classified as Green List (High Evidence).",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:19:03.981522+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GFM1 were changed from to Combined oxidative phosphorylation deficiency 1 MIM#609060",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:18:43.528793+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GFM1 were set to ",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:18:24.859748+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GFM1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GFM1",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:17:20.394316+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GJA3 as ready",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:17:20.382558+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gja3 has been classified as Green List (High Evidence).",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:17:12.957292+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GJA3 were changed from to Cataract 14, multiple types MIM#601885",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:16:54.681921+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GJA3 were set to ",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:16:34.093449+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GJA3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:15:59.802029+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NECTIN4 as ready",
"entity_name": "NECTIN4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:15:59.792794+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nectin4 has been classified as Green List (High Evidence).",
"entity_name": "NECTIN4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:15:52.704206+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NECTIN4 were changed from to Ectodermal dysplasia-syndactyly syndrome 1 (MIM#613573)",
"entity_name": "NECTIN4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:15:34.952854+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NECTIN4 were set to ",
"entity_name": "NECTIN4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:15:16.178778+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NECTIN4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NECTIN4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:14:55.565119+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NECTIN4: Rating: GREEN; Mode of pathogenicity: None; Publications: 24577405, 20691405, 25529316; Phenotypes: Ectodermal dysplasia-syndactyly syndrome 1 (MIM#613573); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NECTIN4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:14:31.517834+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NECTIN4 as ready",
"entity_name": "NECTIN4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:14:31.503968+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nectin4 has been classified as Green List (High Evidence).",
"entity_name": "NECTIN4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:14:05.702121+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NECTIN4 were changed from ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1 to Ectodermal dysplasia-syndactyly syndrome 1 (MIM#613573)",
"entity_name": "NECTIN4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:13:43.286160+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1046",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NECTIN4 were set to ",
"entity_name": "NECTIN4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:13:04.241741+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GJA3 as Green List (high evidence)",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:13:04.231430+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gja3 has been classified as Green List (High Evidence).",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:12:52.022786+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GJA3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cataract 14, multiple types MIM#601885; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:11:43.490598+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GJC2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:11:23.306857+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GJC2 as ready",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:11:23.296254+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gjc2 has been classified as Green List (High Evidence).",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:11:13.847575+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GJC2 were changed from to Spastic paraplegia 44, autosomal recessive MIM#613206; Leukodystrophy, hypomyelinating, 2 MIM#608804; Lymphatic malformation 3 MIM#613480",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:10:53.875259+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GJC2 were set to ",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:10:34.632240+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GJC2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:09:41.831736+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EPHB4 as ready",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:09:41.822347+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ephb4 has been classified as Green List (High Evidence).",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:09:33.136225+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EPHB4 were changed from to Capillary malformation-arteriovenous malformation 2 (MIM#618196), AD; Lymphatic malformation 7 (MIM#617300), AD",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:09:12.427420+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EPHB4 were set to ",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:08:52.423413+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EPHB4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2021-12-06T18:08:34.764698+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EPHB4: Rating: GREEN; Mode of pathogenicity: None; Publications: 27400125, 28687708, 29444212, 29905864, 30578106, 30819650; Phenotypes: Capillary malformation-arteriovenous malformation 2 (MIM#618196), AD, Lymphatic malformation 7 (MIM#617300), AD; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:40:18.979679+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WNT4 as ready",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:40:18.968487+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnt4 has been classified as Amber List (Moderate Evidence).",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:40:10.963625+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WNT4 were changed from to Mullerian aplasia and hyperandrogenism (MIM#158330); SERKAL syndrome, OMIM #611812",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:39:50.521341+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WNT4 were set to ",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:39:28.151707+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WNT4 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:38:38.158792+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: WNT4 as Amber List (moderate evidence)",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:38:38.149708+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnt4 has been classified as Amber List (Moderate Evidence).",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:38:18.743401+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WNT4: Rating: AMBER; Mode of pathogenicity: None; Publications: 22503279, 21377155, 16959810, 18179883, 15317892, 18182450; Phenotypes: Mullerian aplasia and hyperandrogenism (MIM#158330), SERKAL syndrome, OMIM #611812; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:37:06.221411+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WNT4 as ready",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:37:06.211283+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnt4 has been classified as Amber List (Moderate Evidence).",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:37:02.195891+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WNT4 were changed from MULLERIAN APLASIA AND HYPERANDROGENISM; SERKAL SYNDROME to Mullerian aplasia and hyperandrogenism (MIM#158330); SERKAL syndrome, OMIM #611812",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:36:47.163213+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1043",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WNT4 were set to ",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:36:22.077351+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WNT4: Rating: AMBER; Mode of pathogenicity: None; Publications: 22503279, 21377155, 16959810, 18179883; Phenotypes: Mullerian aplasia and hyperandrogenism (MIM#158330), SERKAL syndrome, OMIM #611812; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WNT4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:28:30.155266+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WWOX as ready",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:28:30.144489+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wwox has been classified as Green List (High Evidence).",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:28:22.249190+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WWOX were changed from to Spinocerebellar ataxia, autosomal recessive 12, MIM# 614322; Developmental and epileptic encephalopathy 28, MIM# 616211",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:28:02.927616+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WWOX were set to ",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:27:43.994924+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WWOX was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:27:24.468082+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WWOX: Rating: GREEN; Mode of pathogenicity: None; Publications: 24456803, 25411445, 32051108, 32037574, 24369382, 34831305, 33916893; Phenotypes: Spinocerebellar ataxia, autosomal recessive 12, MIM# 614322, Developmental and epileptic encephalopathy 28, MIM# 616211; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:22:06.633717+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: WWOX.",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:21:28.148611+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WWOX as ready",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:21:28.139642+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wwox has been classified as Green List (High Evidence).",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:21:24.863867+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WWOX were changed from SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 to Developmental and epileptic encephalopathy 28, MIM# 616211",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:21:12.538659+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1041",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WWOX were set to ",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:21:01.176915+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1040",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: WWOX as Green List (high evidence)",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:21:01.167120+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1040",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wwox has been classified as Green List (High Evidence).",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:19:59.481189+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1039",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WWOX: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Developmental and epileptic encephalopathy 28, MIM# 616211; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WWOX",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:19:07.994785+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF750 as ready",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:19:07.983630+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf750 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:18:59.370093+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF750 were changed from to Seborrhea-like dermatitis with psoriasiform elements, MIM# 610227",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:18:40.287324+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZNF750 were set to ",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:18:22.184804+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZNF750 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:18:05.458663+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZNF750 as Red List (low evidence)",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:18:05.448193+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf750 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:17:47.941732+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZNF750: Rating: RED; Mode of pathogenicity: None; Publications: 22185198, 16751772, 22936986; Phenotypes: Seborrhea-like dermatitis with psoriasiform elements, MIM# 610227; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:16:30.828138+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1039",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF750 as ready",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:16:30.817446+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1039",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf750 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:16:26.416265+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1039",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZNF750 were changed from SEBORRHEA-LIKE DERMATITIS WITH PSORIASIFORM ELEMENTS to Seborrhea-like dermatitis with psoriasiform elements, MIM# 610227",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:16:14.260899+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZNF750 were set to ",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:14:42.947292+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1037",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZNF750 as Red List (low evidence)",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:14:42.936531+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1037",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf750 has been classified as Red List (Low Evidence).",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:14:00.666551+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZNF750: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Seborrhea-like dermatitis with psoriasiform elements, MIM# 610227; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZNF750",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:09:56.641643+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SCNN1G as ready",
"entity_name": "SCNN1G",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:09:56.630440+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: scnn1g has been classified as Amber List (Moderate Evidence).",
"entity_name": "SCNN1G",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:09:48.133227+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SCNN1G as Amber List (moderate evidence)",
"entity_name": "SCNN1G",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:09:48.118917+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: scnn1g has been classified as Amber List (Moderate Evidence).",
"entity_name": "SCNN1G",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:08:52.388285+11:00",
"panel_name": "Hydrocephalus_Ventriculomegaly",
"panel_id": 115,
"panel_version": "0.107",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MCIDAS as Green List (high evidence)",
"entity_name": "MCIDAS",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:08:52.377806+11:00",
"panel_name": "Hydrocephalus_Ventriculomegaly",
"panel_id": 115,
"panel_version": "0.107",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mcidas has been classified as Green List (High Evidence).",
"entity_name": "MCIDAS",
"entity_type": "gene"
}
]
}