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{
"count": 220790,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=994",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=992",
"results": [
{
"created": "2022-02-15T12:41:00.367986+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3459",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DBT were changed from MAPLE SYRUP URINE DISEASEQ to Maple syrup urine disease, type II (MIM#248600)",
"entity_name": "DBT",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:40:48.667561+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3458",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DBT were set to ",
"entity_name": "DBT",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:40:17.225987+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3457",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DARS2 as ready",
"entity_name": "DARS2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:40:17.216701+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3457",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dars2 has been classified as Red List (Low Evidence).",
"entity_name": "DARS2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:40:11.772639+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3457",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DARS2 were changed from LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION to Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation, MIM# 611105",
"entity_name": "DARS2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:39:58.517913+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3456",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DARS2 were set to ",
"entity_name": "DARS2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:39:19.282910+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3455",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TTC19 as ready",
"entity_name": "TTC19",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:39:19.267532+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3455",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc19 has been classified as Red List (Low Evidence).",
"entity_name": "TTC19",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:39:13.817983+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3455",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TTC19 were changed from MITOCHONDRIAL COMPLEX III DEFICIENCY to Mitochondrial complex III deficiency, nuclear type 2 (MIM#615157)",
"entity_name": "TTC19",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:39:01.929546+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3454",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TTC19 were set to ",
"entity_name": "TTC19",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:38:08.391573+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP19A1 as ready",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:38:08.380197+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp19a1 has been classified as Red List (Low Evidence).",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:38:04.110705+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP19A1 were changed from Aromatase deficiency 613546; Aromatase excess syndrome 139300 to Aromatase deficiency (MIM#613546), AR; Aromatase excess syndrome (MIM#139300), AD",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:37:50.507228+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3452",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYP19A1 were set to ",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:37:39.479379+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3451",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CYP19A1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CYP19A1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:37:05.023790+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3450",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNXB as ready",
"entity_name": "TNXB",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:37:04.997533+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3450",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnxb has been classified as Red List (Low Evidence).",
"entity_name": "TNXB",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:36:44.280535+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3450",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNXB were set to ",
"entity_name": "TNXB",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:36:27.228798+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3449",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNXB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Vesicoureteral reflux 8, MIM#615963; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNXB",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:33:52.863808+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FTSJ1 as ready",
"entity_name": "FTSJ1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:33:52.851673+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ftsj1 has been classified as Green List (High Evidence).",
"entity_name": "FTSJ1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:33:45.415423+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FTSJ1 were changed from to Intellectual developmental disorder, X-linked 9 MIM#309549",
"entity_name": "FTSJ1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:33:25.405990+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10971",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FTSJ1 were set to ",
"entity_name": "FTSJ1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:32:28.987660+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FTSJ1 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "FTSJ1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:31:51.985141+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3449",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FLRT3 as ready",
"entity_name": "FLRT3",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:31:51.972875+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3449",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: flrt3 has been classified as Red List (Low Evidence).",
"entity_name": "FLRT3",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:31:47.606202+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3449",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FLRT3 were changed from Hypogonadotropic hypogonadism 21 with anosmia 615271 to Hypogonadotropic hypogonadism 21 with anosmia (MIM# 615271)",
"entity_name": "FLRT3",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:31:34.928988+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3448",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FLRT3 were set to ",
"entity_name": "FLRT3",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:31:23.845914+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3447",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FLRT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FLRT3",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:30:51.457347+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3446",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMEM126B as ready",
"entity_name": "TMEM126B",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:30:51.443843+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3446",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem126b has been classified as Amber List (Moderate Evidence).",
"entity_name": "TMEM126B",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:30:47.659903+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3446",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM126B were changed from Muscle Weakness and Isolated Complex I Deficiency to Mitochondrial complex I deficiency, nuclear type 29 (MIM#618250)",
"entity_name": "TMEM126B",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:30:35.265118+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMEM126B were set to ",
"entity_name": "TMEM126B",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:30:23.596520+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TMEM126B as Amber List (moderate evidence)",
"entity_name": "TMEM126B",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:30:23.582031+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem126b has been classified as Amber List (Moderate Evidence).",
"entity_name": "TMEM126B",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:28:55.387531+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FLAD1 as ready",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:28:55.374816+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: flad1 has been classified as Green List (High Evidence).",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:28:47.552292+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FLAD1 were changed from to Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency MIM#255100",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:28:27.609051+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10968",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FLAD1 were set to ",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:28:08.282285+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10967",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FLAD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:27:34.342211+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3443",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FLAD1 as ready",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:27:34.332191+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3443",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: flad1 has been classified as Red List (Low Evidence).",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:27:30.809744+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3443",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FLAD1 were changed from Riboflavin-Responsive and Non-responsive Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency. to Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency MIM#255100",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:27:15.214996+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FLAD1 were set to ",
"entity_name": "FLAD1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:26:45.231098+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TK2 as ready",
"entity_name": "TK2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:26:45.216199+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tk2 has been classified as Red List (Low Evidence).",
"entity_name": "TK2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:26:41.098811+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TK2 were changed from MITOCHONDRIAL DNA DEPLETION SYNDROME, MYOPATHIC FORM to Mitochondrial DNA depletion syndrome 2 (myopathic type) (MIM#609560)",
"entity_name": "TK2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:26:01.363721+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3440",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGF20 as ready",
"entity_name": "FGF20",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:26:01.353450+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3440",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgf20 has been classified as Amber List (Moderate Evidence).",
"entity_name": "FGF20",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:25:57.562766+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3440",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FGF20 were changed from ?Renal hypodysplasia/aplasia 2, 615721 to Renal hypodysplasia/aplasia 2, MIM#615721",
"entity_name": "FGF20",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:25:25.474591+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3439",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FGF20 as Amber List (moderate evidence)",
"entity_name": "FGF20",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:25:25.455570+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3439",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgf20 has been classified as Amber List (Moderate Evidence).",
"entity_name": "FGF20",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:24:40.120927+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGF17 as ready",
"entity_name": "FGF17",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:24:40.109309+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgf17 has been classified as Red List (Low Evidence).",
"entity_name": "FGF17",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:24:34.313571+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FGF17 were set to ",
"entity_name": "FGF17",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:24:22.118504+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FGF17 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGF17",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:23:52.061239+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TEK as ready",
"entity_name": "TEK",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:23:52.050745+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tek has been classified as Red List (Low Evidence).",
"entity_name": "TEK",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:23:48.494407+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TEK were changed from VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL to Glaucoma 3, primary congenital, E (MIM#617272); Venous malformations, multiple cutaneous and mucosal (MIM#600195)",
"entity_name": "TEK",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:23:35.297477+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3435",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TEK were set to ",
"entity_name": "TEK",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:22:37.626095+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGF17 as ready",
"entity_name": "FGF17",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:22:37.614678+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgf17 has been classified as Green List (High Evidence).",
"entity_name": "FGF17",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:22:19.955114+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FGF17 were changed from to Hypogonadotropic hypogonadism 20 with or without anosmia MIM#615270",
"entity_name": "FGF17",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:21:57.225396+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10965",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FGF17 were set to ",
"entity_name": "FGF17",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:21:10.607069+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FGF17 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FGF17",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:12:20.442658+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBXAS1 were changed from Ghosal hematodiaphyseal syndrome (MIM#231095) to Ghosal haematodiaphyseal syndrome (MIM#231095)",
"entity_name": "TBXAS1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:12:07.831659+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBXAS1 as ready",
"entity_name": "TBXAS1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:12:07.819596+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbxas1 has been classified as Red List (Low Evidence).",
"entity_name": "TBXAS1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:12:04.226770+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBXAS1 were changed from GHOSAL HEMATODIAPHYSEAL SYNDROME to Ghosal hematodiaphyseal syndrome (MIM#231095)",
"entity_name": "TBXAS1",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:11:25.711356+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3432",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TANGO2 as ready",
"entity_name": "TANGO2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:11:25.700020+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3432",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tango2 has been classified as Red List (Low Evidence).",
"entity_name": "TANGO2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:11:21.628732+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3432",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TANGO2 were changed from Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy to Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration (MIM#616878)",
"entity_name": "TANGO2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:11:06.053455+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3431",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TANGO2 were set to ",
"entity_name": "TANGO2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:10:49.506813+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TANGO2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration (MIM#616878); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TANGO2",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:10:06.144795+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZFYVE26 as ready",
"entity_name": "ZFYVE26",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:10:06.130882+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zfyve26 has been classified as Red List (Low Evidence).",
"entity_name": "ZFYVE26",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:10:01.852802+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZFYVE26 were changed from SPASTIC PARAPLEGIA AUTOSOMAL RECESSIVE TYPE 15 to Spastic paraplegia 15, autosomal recessive MIM#270700",
"entity_name": "ZFYVE26",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:09:47.227318+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3429",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZFYVE26 were set to ",
"entity_name": "ZFYVE26",
"entity_type": "gene"
},
{
"created": "2022-02-15T12:09:28.596111+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZFYVE26: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Spastic paraplegia 15, autosomal recessive MIM#270700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZFYVE26",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:50:18.109844+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4503",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SYP as ready",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:50:18.098436+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4503",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: syp has been classified as Green List (High Evidence).",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:50:02.946964+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4503",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SYP were changed from to Mental retardation, X-linked 96 MIM#300802",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:49:28.472018+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SYP were set to ",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:48:54.570295+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4501",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SYP was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:48:21.879772+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4500",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SYP: Rating: GREEN; Mode of pathogenicity: None; Publications: 23966691, 19377476; Phenotypes: Mental retardation, X-linked 96 MIM#300802; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:46:53.166951+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10963",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SYP as ready",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:46:53.157655+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10963",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: syp has been classified as Green List (High Evidence).",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:46:45.656303+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10963",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SYP were changed from to Mental retardation, X-linked 96 MIM#300802",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:46:24.984121+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SYP were set to ",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:46:05.307457+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: SYP was changed from to None",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:45:47.134746+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SYP was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:44:48.706769+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SYP as ready",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:44:48.683270+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: syp has been classified as Red List (Low Evidence).",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:44:45.216258+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SYP were changed from MENTAL RETARDATION X-LINKED SYP-RELATED to Intellectual developmental disorder, X-linked 96 (MIM#300802)",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:44:32.875920+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SYP were set to ",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:44:17.855480+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SYP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "SYP",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:43:34.759749+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYC1 as ready",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:43:34.750302+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyc1 has been classified as Red List (Low Evidence).",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:43:31.248042+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYC1 were changed from MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 to Mitochondrial complex III deficiency, nuclear type 6, MIM# 615453",
"entity_name": "CYC1",
"entity_type": "gene"
},
{
"created": "2022-02-15T11:43:19.018244+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.3425",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CYC1 were set to ",
"entity_name": "CYC1",
"entity_type": "gene"
}
]
}