HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1096",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1094",
"results": [
{
"created": "2021-12-06T17:08:18.881347+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1035",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MCIDAS as ready",
"entity_name": "MCIDAS",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:08:18.870512+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1035",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mcidas has been classified as Green List (High Evidence).",
"entity_name": "MCIDAS",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:08:00.404590+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1035",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MCIDAS as Green List (high evidence)",
"entity_name": "MCIDAS",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:08:00.392354+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1035",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mcidas has been classified as Green List (High Evidence).",
"entity_name": "MCIDAS",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:07:55.909875+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic",
"panel_id": 63,
"panel_version": "0.98",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: GDF6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: syndromic CAKUT; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "GDF6",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:05:48.924427+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GDF6 as ready",
"entity_name": "GDF6",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:05:48.914912+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gdf6 has been classified as Green List (High Evidence).",
"entity_name": "GDF6",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:05:44.622836+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GDF6 were changed from KLIPPEL-FEIL SYNDROME TYPE 1; MICROPHTHALMIA ISOLATED TYPE 4; Syndromic CAKUT to Multiple synostoses syndrome 4 (MIM#617898)",
"entity_name": "GDF6",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:05:31.212138+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: GDF6 was changed from to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
"entity_name": "GDF6",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:03:04.444582+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GJC2 as ready",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:03:04.433706+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1032",
"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": "2021-12-06T17:02:58.720133+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GLA as ready",
"entity_name": "GLA",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:02:58.709158+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gla has been classified as Red List (Low Evidence).",
"entity_name": "GLA",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:02:51.400056+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GJC2 were changed from LYMPHEDEMA, HEREDITARY, IC; SPASTIC PARAPLEGIA, 44; LEUKODYSTROPHY, HYPOMYELINATING, 2 to Leukodystrophy, hypomyelinating, 2 MIM#608804",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:02:36.713125+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GJC2 were set to ",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:02:25.151640+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1030",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GJC2 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:02:10.896077+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1029",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: GJA3 as ready",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:02:10.883575+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1029",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: gja3 has been classified as Red List (Low Evidence).",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:02:07.815767+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1029",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GJC2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukodystrophy, hypomyelinating, 2 MIM#608804; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GJC2",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:02:04.823843+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1029",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: GJA3 were changed from CATARACT ZONULAR PULVERULENT CATARACT TYPE 3 to Cataract 14, multiple types MIM#601885",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:01:52.055247+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1028",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Mode of inheritance for gene: GJA3 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:01:37.826379+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1027",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Classified gene: GJA3 as Red List (low evidence)",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:01:37.816126+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1027",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: gja3 has been classified as Red List (Low Evidence).",
"entity_name": "GJA3",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:01:02.070167+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1026",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: EPHB4 as ready",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:01:02.056295+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1026",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: ephb4 has been classified as Green List (High Evidence).",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:00:55.688699+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1026",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: EPHB4 were changed from hydrops fetalis gene to Capillary malformation-arteriovenous malformation 2 (MIM#618196), AD; Lymphatic malformation 7 (MIM#617300), AD; hydrops fetalis",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:00:29.232980+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1025",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: EPHB4 were set to 27400125",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2021-12-06T17:00:09.021543+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1024",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Mode of inheritance for gene: EPHB4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:58:41.173688+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1023",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAJB13 as ready",
"entity_name": "DNAJB13",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:58:41.162913+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1023",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajb13 has been classified as Red List (Low Evidence).",
"entity_name": "DNAJB13",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:58:37.646675+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1023",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GLA were set to ",
"entity_name": "GLA",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:58:10.553743+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1022",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GLA as Red List (low evidence)",
"entity_name": "GLA",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:58:10.543093+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1022",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gla has been classified as Red List (Low Evidence).",
"entity_name": "GLA",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:58:04.280428+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1021",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: GAS2L2 as ready",
"entity_name": "GAS2L2",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:58:04.269670+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1021",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: gas2l2 has been classified as Red List (Low Evidence).",
"entity_name": "GAS2L2",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:57:52.905618+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1021",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Classified gene: GAS2L2 as Red List (low evidence)",
"entity_name": "GAS2L2",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:57:52.885886+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1021",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: gas2l2 has been classified as Red List (Low Evidence).",
"entity_name": "GAS2L2",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:57:17.056193+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GLB1 as ready",
"entity_name": "GLB1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:57:17.044610+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: glb1 has been classified as Green List (High Evidence).",
"entity_name": "GLB1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:57:15.090473+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1020",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: NBAS as ready",
"entity_name": "NBAS",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:57:15.066463+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1020",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: nbas has been classified as Green List (High Evidence).",
"entity_name": "NBAS",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:57:09.345968+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1020",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DNAJB13 as Red List (low evidence)",
"entity_name": "DNAJB13",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:57:09.328644+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1020",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajb13 has been classified as Red List (Low Evidence).",
"entity_name": "DNAJB13",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:57:06.380550+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1019",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: NBAS were changed from ACUTE LIVER FAILURE (ALF) IN INFANCY AND CHILDHOOD to Short stature, optic nerve atrophy, and Pelger-Huet anomaly (MIM#614800); bone fragility; developmental delay; immunodeficiency; autism",
"entity_name": "NBAS",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:57:01.788690+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GLB1 were changed from to GM1-gangliosidosis, type I MIM#230500; GM1-gangliosidosis, type II MIM# 230600; GM1-gangliosidosis, type III MIM#230650; Mucopolysaccharidosis type IVB (Morquio) MIM#253010",
"entity_name": "GLB1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:56:39.456521+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GLB1 were set to ",
"entity_name": "GLB1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:56:32.316475+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1018",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: NBAS were set to ",
"entity_name": "NBAS",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:55:58.059111+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GLB1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GLB1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:55:16.439725+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1017",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: DNAH8 as ready",
"entity_name": "DNAH8",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:55:16.428581+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1017",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: dnah8 has been classified as Red List (Low Evidence).",
"entity_name": "DNAH8",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:55:05.603508+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1017",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: DNAH8 were changed from Spermatogenic failure 46 - OMIM# 619095; primary ciliary dyskinesia to primary ciliary dyskinesia",
"entity_name": "DNAH8",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:54:59.895560+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1016",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GLB1 as ready",
"entity_name": "GLB1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:54:59.885374+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1016",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: glb1 has been classified as Green List (High Evidence).",
"entity_name": "GLB1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:54:54.816932+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1016",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GLB1 were changed from GM1-GANGLIOSIDOSIS TYPE 1; GM1-GANGLIOSIDOSIS TYPE 2; GM1-GANGLIOSIDOSIS TYPE 3; MUCOPOLYSACCHARIDOSIS TYPE 4B to GM1-gangliosidosis, type I MIM#230500; GM1-gangliosidosis, type II MIM# 230600; GM1-gangliosidosis, type III MIM#230650; Mucopolysaccharidosis type IVB (Morquio) MIM#253010",
"entity_name": "GLB1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:54:46.690505+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1015",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Classified gene: DNAH8 as Red List (low evidence)",
"entity_name": "DNAH8",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:54:46.680255+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1015",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: dnah8 has been classified as Red List (Low Evidence).",
"entity_name": "DNAH8",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:54:30.881096+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1014",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAH6 as ready",
"entity_name": "DNAH6",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:54:30.870711+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1014",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnah6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DNAH6",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:54:23.404169+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1014",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DNAH6 were changed from heterotaxy; azoospermia to Heterotaxy",
"entity_name": "DNAH6",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:54:03.569073+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1013",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DNAH6 as Amber List (moderate evidence)",
"entity_name": "DNAH6",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:54:03.514368+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1013",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnah6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DNAH6",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:53:18.639393+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1012",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: DNAH1 as ready",
"entity_name": "DNAH1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:53:18.622666+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1012",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: dnah1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DNAH1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:53:05.712642+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1012",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: DNAH1 were changed from Situs inversus; primary ciliary dyskinesia; infertility to Situs inversus; primary ciliary dyskinesia, MIM#617577; infertility, MIM#617576",
"entity_name": "DNAH1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:51:09.118022+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1011",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Classified gene: DNAH1 as Amber List (moderate evidence)",
"entity_name": "DNAH1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:51:09.107002+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1011",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: dnah1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DNAH1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:51:00.393484+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.126",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: LACC1 as ready",
"entity_name": "LACC1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:51:00.381358+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.126",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: lacc1 has been classified as Green List (High Evidence).",
"entity_name": "LACC1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:50:42.283388+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1010",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GLB1 were set to ",
"entity_name": "GLB1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:50:36.114342+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.126",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: LACC1 as Green List (high evidence)",
"entity_name": "LACC1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:50:36.103841+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.126",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: lacc1 has been classified as Green List (High Evidence).",
"entity_name": "LACC1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:49:32.300555+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1009",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GLDC as ready",
"entity_name": "GLDC",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:49:32.289952+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1009",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gldc has been classified as Amber List (Moderate Evidence).",
"entity_name": "GLDC",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:49:28.261322+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1009",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GLDC were changed from GLDC-RELATED GLYCINE ENCEPHALOPATHY to Glycine encephalopathy (MIM#605899)",
"entity_name": "GLDC",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:49:20.929694+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1008",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: GLI2 as ready",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:49:20.920221+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1008",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: gli2 has been classified as Green List (High Evidence).",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:49:15.194134+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1008",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GLDC were set to ",
"entity_name": "GLDC",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:49:09.764558+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1007",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: GLI2 were changed from GLI2-RELATED HOLOPROSENCEPHALY to Culler-Jones syndrome, MIM#615849; Holoprosencephaly 9, MIM# 61082",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:49:03.349772+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1006",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GLDC as Amber List (moderate evidence)",
"entity_name": "GLDC",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:49:03.338729+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1006",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gldc has been classified as Amber List (Moderate Evidence).",
"entity_name": "GLDC",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:48:55.456981+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1005",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Mode of inheritance for gene: GLI2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:48:40.151628+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1004",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: GLI2 were set to ",
"entity_name": "GLI2",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:48:06.801894+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1003",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EP300 as ready",
"entity_name": "EP300",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:48:06.792425+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1003",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ep300 has been classified as Green List (High Evidence).",
"entity_name": "EP300",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:48:02.713689+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1003",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EP300 were changed from RUBINSTEIN-TAYBI SYNDROME TYPE 2 to Rubinstein-Taybi syndrome 2, MIM# 613684; Menke-Hennekam syndrome , MIM#2 618333",
"entity_name": "EP300",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:47:48.105436+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1002",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EP300 were set to ",
"entity_name": "EP300",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:47:36.052222+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1001",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EP300 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EP300",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:46:56.464164+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1000",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CFAP57 as ready",
"entity_name": "CFAP57",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:46:56.449038+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1000",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cfap57 has been classified as Red List (Low Evidence).",
"entity_name": "CFAP57",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:46:38.031106+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1000",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NANS as ready",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:46:38.020804+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1000",
"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": "2021-12-06T16:46:36.645765+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.125",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "gene: LACC1 was added\ngene: LACC1 was added to Systemic Autoinflammatory Disease_Periodic Fever. Sources: Literature\nMode of inheritance for gene: LACC1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: LACC1 were set to 25220867; 27881174; 30872671; 33718577\nPhenotypes for gene: LACC1 were set to Juvenile arthritis MIM#618795\nReview for gene: LACC1 was set to GREEN\nAdded comment: At least 43 cases with biallelic variants (7 different variants) from 17 mainly consanguineous families reported. At least 10 of the families had systemic disease, which all demonstrated increased inflammatory markers. \nSources: Literature",
"entity_name": "LACC1",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:46:30.834251+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1000",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NANS were changed from infantile-onset severe developmental delay and skeletal dysplasia to Spondyloepimetaphyseal dysplasia, Camera-Genevieve type (MIM#610442)",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:46:19.280418+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.999",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NANS were set to ",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:46:02.395687+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.998",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Marked gene: NALCN as ready",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:46:02.384926+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.998",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Gene: nalcn has been classified as Green List (High Evidence).",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:45:55.890906+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.998",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Phenotypes for gene: NALCN were changed from HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES; CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY; SEVERE HYPOTONIA, SPEECH IMPAIRMENT, AND COGNITIVE DELAY to Congenital contractures of the limbs and face, hypotonia, and developmental delay (MIM#616266); Hypotonia, infantile, with psychomotor retardation and characteristic facies 1 (MIM#615419)",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:45:42.126129+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.997",
"user_name": "Seb Lunke",
"item_type": "entity",
"text": "Publications for gene: NALCN were set to ",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:45:33.542026+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.996",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CFAP57 as Red List (low evidence)",
"entity_name": "CFAP57",
"entity_type": "gene"
},
{
"created": "2021-12-06T16:45:33.531703+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.996",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cfap57 has been classified as Red List (Low Evidence).",
"entity_name": "CFAP57",
"entity_type": "gene"
}
]
}