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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1120",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1118",
"results": [
{
"created": "2021-11-22T21:26:16.088164+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9843",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DVL3 as ready",
"entity_name": "DVL3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:26:16.077295+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9843",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dvl3 has been classified as Green List (High Evidence).",
"entity_name": "DVL3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:26:08.706194+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9843",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DVL3 were changed from to Robinow syndrome, autosomal dominant 3 MIM#616894",
"entity_name": "DVL3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:25:47.904657+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9842",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DVL3 were set to ",
"entity_name": "DVL3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:25:25.948096+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9841",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DVL3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DVL3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:25:07.891042+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9840",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DVL3: Rating: GREEN; Mode of pathogenicity: None; Publications: 26924530; Phenotypes: Robinow syndrome, autosomal dominant 3 MIM#616894; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DVL3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:24:56.089837+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DVL3 as ready",
"entity_name": "DVL3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:24:56.080030+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dvl3 has been classified as Green List (High Evidence).",
"entity_name": "DVL3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:24:52.212611+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DVL3 were changed from AUTOSOMAL-DOMINANT ROBINOW SYNDROME to Robinow syndrome, autosomal dominant 3 MIM#616894",
"entity_name": "DVL3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:24:39.660317+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.683",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DVL3 were set to ",
"entity_name": "DVL3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:24:11.934728+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DVL3 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DVL3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:23:19.809837+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.681",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EN1 as ready",
"entity_name": "EN1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:23:19.799625+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.681",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: en1 has been classified as Green List (High Evidence).",
"entity_name": "EN1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:23:14.919283+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.681",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: EN1.\nTag 5'UTR tag was added to gene: EN1.",
"entity_name": "EN1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:22:49.546275+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.681",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EN1 were changed from ?ENDOVE syndrome, limb-brain type - OMIM#619218 to ENDOVE syndrome, limb-brain type - OMIM#619218",
"entity_name": "EN1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:22:37.626881+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EN1 as Green List (high evidence)",
"entity_name": "EN1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:22:37.615825+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: en1 has been classified as Green List (High Evidence).",
"entity_name": "EN1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:21:58.233572+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.679",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC30A5 as ready",
"entity_name": "SLC30A5",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:21:58.223380+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.679",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc30a5 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SLC30A5",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:21:51.208502+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.679",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC30A5 as Amber List (moderate evidence)",
"entity_name": "SLC30A5",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:21:51.195443+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.679",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc30a5 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SLC30A5",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:21:13.744830+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.678",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SCN5A as ready",
"entity_name": "SCN5A",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:21:13.726343+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.678",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: scn5a has been classified as Green List (High Evidence).",
"entity_name": "SCN5A",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:21:07.403718+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.678",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SCN5A as Green List (high evidence)",
"entity_name": "SCN5A",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:21:07.393060+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.678",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: scn5a has been classified as Green List (High Evidence).",
"entity_name": "SCN5A",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:20:42.720127+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRF1 as ready",
"entity_name": "PRF1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:20:42.708418+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prf1 has been classified as Green List (High Evidence).",
"entity_name": "PRF1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:20:39.096880+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRF1 were changed from Aplastic anemia - #609135; Hemophagocytic lymphohistiocytosis, familial, 2 - #603553 to Aplastic anaemia - #609135; Haemophagocytic lymphohistiocytosis, familial, 2 - #603553",
"entity_name": "PRF1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:20:21.411273+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.676",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PRF1 as Green List (high evidence)",
"entity_name": "PRF1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:20:21.402386+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.676",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prf1 has been classified as Green List (High Evidence).",
"entity_name": "PRF1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:19:51.396160+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.675",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GATA1 as ready",
"entity_name": "GATA1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:19:51.384815+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.675",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gata1 has been classified as Green List (High Evidence).",
"entity_name": "GATA1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:19:46.699302+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.675",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GATA1 were changed from Anaemia, X-linked, with/without neutropenia and/or platelet abnormalities, MIM#300835 to Anaemia, X-linked, with/without neutropaenia and/or platelet abnormalities, MIM#300835",
"entity_name": "GATA1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:19:35.837484+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.674",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GATA1 were changed from Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, MIM#300835 to Anaemia, X-linked, with/without neutropenia and/or platelet abnormalities, MIM#300835",
"entity_name": "GATA1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:19:19.964141+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GATA1 as Green List (high evidence)",
"entity_name": "GATA1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:19:19.953363+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gata1 has been classified as Green List (High Evidence).",
"entity_name": "GATA1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:18:45.352606+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALPK3 as ready",
"entity_name": "ALPK3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:18:45.342820+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alpk3 has been classified as Green List (High Evidence).",
"entity_name": "ALPK3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:18:39.802897+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ALPK3 as Green List (high evidence)",
"entity_name": "ALPK3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:18:39.792396+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alpk3 has been classified as Green List (High Evidence).",
"entity_name": "ALPK3",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:18:13.503380+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZBTB42 as ready",
"entity_name": "ZBTB42",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:18:13.491363+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zbtb42 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ZBTB42",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:18:09.553279+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZBTB42 were changed from ?Lethal congenital contracture syndrome 6- #616248 to Lethal congenital contracture syndrome 6- #616248",
"entity_name": "ZBTB42",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:17:58.043469+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZBTB42 as Amber List (moderate evidence)",
"entity_name": "ZBTB42",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:17:58.033267+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zbtb42 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ZBTB42",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:17:25.789523+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UNC50 as ready",
"entity_name": "UNC50",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:17:25.778777+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: unc50 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UNC50",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:17:22.289929+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UNC50 were changed from to Arthrogryposis multiplex congenita",
"entity_name": "UNC50",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:17:09.370936+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UNC50 as Amber List (moderate evidence)",
"entity_name": "UNC50",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:17:09.358807+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: unc50 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UNC50",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:16:57.700982+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: UNC50: Added comment: Supportive functional data.; Changed rating: AMBER",
"entity_name": "UNC50",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:16:14.819901+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UNC50: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "UNC50",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:15:45.357350+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TOR1AIP1 as ready",
"entity_name": "TOR1AIP1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:15:45.347299+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tor1aip1 has been classified as Green List (High Evidence).",
"entity_name": "TOR1AIP1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:15:42.066497+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TOR1AIP1 were changed from ?Muscular dystrophy, autosomal recessive, with rigid spine and distal joint contractures - #61707; congenital myasthenic syndrome to Muscular dystrophy, autosomal recessive, with rigid spine and distal joint contractures - #61707; congenital myasthenic syndrome",
"entity_name": "TOR1AIP1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:15:29.595324+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TOR1AIP1 as Green List (high evidence)",
"entity_name": "TOR1AIP1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:15:29.585241+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tor1aip1 has been classified as Green List (High Evidence).",
"entity_name": "TOR1AIP1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:15:15.175019+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.665",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TOR1AIP1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "TOR1AIP1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:14:23.884215+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.665",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STIM1 as ready",
"entity_name": "STIM1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:14:23.873571+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.665",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stim1 has been classified as Green List (High Evidence).",
"entity_name": "STIM1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:14:18.785739+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.665",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: STIM1 as Green List (high evidence)",
"entity_name": "STIM1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:14:18.776635+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.665",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stim1 has been classified as Green List (High Evidence).",
"entity_name": "STIM1",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:13:23.768697+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SCYL2 as ready",
"entity_name": "SCYL2",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:13:23.757828+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: scyl2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SCYL2",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:13:18.389307+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SCYL2 as Amber List (moderate evidence)",
"entity_name": "SCYL2",
"entity_type": "gene"
},
{
"created": "2021-11-22T21:13:18.370865+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: scyl2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SCYL2",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:11:40.711225+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.663",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIP5K1C as ready",
"entity_name": "PIP5K1C",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:11:40.699772+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.663",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pip5k1c has been classified as Amber List (Moderate Evidence).",
"entity_name": "PIP5K1C",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:11:19.726847+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.663",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PIP5K1C as Amber List (moderate evidence)",
"entity_name": "PIP5K1C",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:11:19.700607+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.663",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pip5k1c has been classified as Amber List (Moderate Evidence).",
"entity_name": "PIP5K1C",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:10:44.964244+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ORAI1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "ORAI1",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:09:51.226790+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ORAI1 as ready",
"entity_name": "ORAI1",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:09:51.212215+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: orai1 has been classified as Green List (High Evidence).",
"entity_name": "ORAI1",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:09:39.588569+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ORAI1 as Green List (high evidence)",
"entity_name": "ORAI1",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:09:39.577717+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: orai1 has been classified as Green List (High Evidence).",
"entity_name": "ORAI1",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:08:50.792031+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.661",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYLPF as ready",
"entity_name": "MYLPF",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:08:50.776106+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.661",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mylpf has been classified as Amber List (Moderate Evidence).",
"entity_name": "MYLPF",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:08:41.750111+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.661",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MYLPF as Amber List (moderate evidence)",
"entity_name": "MYLPF",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:08:41.739598+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.661",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mylpf has been classified as Amber List (Moderate Evidence).",
"entity_name": "MYLPF",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:08:28.958475+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.660",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYLPF: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "MYLPF",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:07:06.670043+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9840",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IRF6 as ready",
"entity_name": "IRF6",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:07:06.659010+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9840",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: irf6 has been classified as Green List (High Evidence).",
"entity_name": "IRF6",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:06:58.723451+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9840",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IRF6 were changed from Popliteal pterygium syndrome 1MIM#119500; van der Woude syndrome MIM#119300 to Popliteal pterygium syndrome 1MIM#119500; van der Woude syndrome MIM#119300",
"entity_name": "IRF6",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:06:40.265449+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9839",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IRF6 were set to 20301581",
"entity_name": "IRF6",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:06:25.091103+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9838",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IRF6 as ready",
"entity_name": "IRF6",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:06:25.080831+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9838",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: irf6 has been classified as Green List (High Evidence).",
"entity_name": "IRF6",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:06:16.916488+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9838",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IRF6 were changed from to Popliteal pterygium syndrome 1MIM#119500; van der Woude syndrome MIM#119300",
"entity_name": "IRF6",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:05:57.463301+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9837",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IRF6 were set to ",
"entity_name": "IRF6",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:05:30.528610+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9836",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IRF6 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "IRF6",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:04:21.029160+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MATN3 as ready",
"entity_name": "MATN3",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:04:21.017893+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: matn3 has been classified as Green List (High Evidence).",
"entity_name": "MATN3",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:04:13.226737+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MATN3 were changed from to Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type (MIM#608728); Epiphyseal dysplasia, multiple, 5 (MIM#607078)",
"entity_name": "MATN3",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:03:49.808271+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9834",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MATN3 were set to ",
"entity_name": "MATN3",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:02:11.639736+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9833",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MATN3 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
"entity_name": "MATN3",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:01:02.273775+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9832",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: INPPL1 as ready",
"entity_name": "INPPL1",
"entity_type": "gene"
},
{
"created": "2021-11-22T20:01:02.243075+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9832",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: inppl1 has been classified as Green List (High Evidence).",
"entity_name": "INPPL1",
"entity_type": "gene"
},
{
"created": "2021-11-22T18:45:03.546898+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9832",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: INPPL1 were changed from to Opsismodysplasia MIM#258480",
"entity_name": "INPPL1",
"entity_type": "gene"
},
{
"created": "2021-11-22T18:44:41.984163+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9831",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: INPPL1 were set to ",
"entity_name": "INPPL1",
"entity_type": "gene"
},
{
"created": "2021-11-22T18:44:23.097362+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9830",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: INPPL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "INPPL1",
"entity_type": "gene"
},
{
"created": "2021-11-22T18:43:54.400976+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: INPPL1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "INPPL1",
"entity_type": "gene"
}
]
}