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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1118",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1116",
"results": [
{
"created": "2021-11-25T18:09:14.824310+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.314",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYGC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:08:49.718455+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYGC: Rating: GREEN; Mode of pathogenicity: None; Publications: 10521291, 10914683, 12011157, 19204787, 22052681; Phenotypes: Cataract 2, multiple types, MIM# 604307; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:08:11.962086+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9877",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYGC as ready",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:08:11.953390+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9877",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crygc has been classified as Green List (High Evidence).",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:08:04.104894+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9877",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYGC were changed from to Cataract 2, multiple types, MIM# 604307",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:07:42.777138+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9876",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYGC were set to ",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:07:19.210720+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9875",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYGC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:07:01.962808+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9874",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYGC: Rating: GREEN; Mode of pathogenicity: None; Publications: 10521291, 10914683, 12011157, 19204787, 22052681; Phenotypes: Cataract 2, multiple types, MIM# 604307; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:06:06.853987+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.712",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYGC as ready",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:06:06.844348+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.712",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crygc has been classified as Green List (High Evidence).",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:06:02.412595+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.712",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYGC were changed from CATARACT AUTOSOMAL DOMINANT to Cataract 2, multiple types, MIM# 604307",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:05:48.815717+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYGC were set to ",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:05:34.383433+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.710",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYGC was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:05:21.498976+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.709",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYGC: Rating: GREEN; Mode of pathogenicity: None; Publications: 10521291, 10914683, 12011157, 19204787, 22052681; Phenotypes: Cataract 2, multiple types, MIM# 604307; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYGC",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:02:28.727603+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYBB3 as ready",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:02:28.718772+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crybb3 has been classified as Green List (High Evidence).",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:02:25.876223+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYBB3 were changed from to Cataract 22, MIM# 609741",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:01:55.815663+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.312",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYBB3 were set to ",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:01:25.346691+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.311",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYBB3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:00:57.648163+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.310",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYBB3: Rating: GREEN; Mode of pathogenicity: None; Publications: 15914629, 23508780, 34356085, 33594837, 33510601; Phenotypes: Cataract 22, MIM# 609741; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:00:15.828168+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9874",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYBB3 as ready",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:00:15.793144+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9874",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crybb3 has been classified as Green List (High Evidence).",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T18:00:02.378631+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9874",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYBB3 were changed from to Cataract 22, MIM# 609741",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:59:40.808412+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9873",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYBB3 were set to ",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:56:02.499114+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9872",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYBB3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:55:42.982690+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9871",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYBB3: Rating: GREEN; Mode of pathogenicity: None; Publications: 15914629, 23508780, 34356085, 33594837, 33510601; Phenotypes: Cataract 22, MIM# 609741; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:54:56.024846+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.709",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYBB3 as ready",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:54:56.015327+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.709",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crybb3 has been classified as Green List (High Evidence).",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:54:52.531278+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.709",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYBB3 were changed from CATARACT, CONGENITAL NUCLEAR, AUTOSOMAL RECESSIVE 2 to Cataract 22, MIM# 609741",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:51:19.755713+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYBB3 were set to ",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:51:08.146823+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.707",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYBB3 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:50:54.723980+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.706",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYBB3: Rating: GREEN; Mode of pathogenicity: None; Publications: 15914629, 23508780, 34356085, 33594837, 33510601; Phenotypes: Cataract 22, MIM# 609741; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CRYBB3",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:48:23.582147+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.310",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYBB2 as ready",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:48:23.571867+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.310",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crybb2 has been classified as Green List (High Evidence).",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:47:43.043675+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.310",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYBB2 were changed from to Cataract 3, multiple types, MIM# 601547",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:47:12.252828+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.309",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYBB2 were set to ",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:46:47.984807+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.308",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYBB2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:46:17.744148+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYBB2: Rating: GREEN; Mode of pathogenicity: None; Publications: 9158139, 10634616, 11424921, 17234267; Phenotypes: Cataract 3, multiple types, MIM# 601547; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:45:40.720780+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9871",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYBB2 as ready",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:45:40.710166+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9871",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crybb2 has been classified as Green List (High Evidence).",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:45:28.412090+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9871",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYBB2 were changed from to Cataract 3, multiple types, MIM# 601547",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:45:11.462542+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9870",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYBB2 were set to ",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:44:52.612270+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9869",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYBB2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:44:19.374034+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9868",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYBB2: Rating: GREEN; Mode of pathogenicity: None; Publications: 9158139, 10634616, 11424921, 17234267; Phenotypes: Cataract 3, multiple types, MIM# 601547; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:43:34.052532+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.706",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYBB2 as ready",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:43:34.041662+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.706",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crybb2 has been classified as Green List (High Evidence).",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:43:30.587932+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.706",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYBB2 were changed from CATARACT, COPPOCK-LIKE; CATARACT, CONGENITAL, CERULEAN TYPE, 2 to Cataract 3, multiple types, MIM# 601547",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:43:10.614955+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYBB2 were set to ",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:42:59.033193+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.704",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYBB2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:42:46.521845+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.703",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYBB2: Rating: GREEN; Mode of pathogenicity: None; Publications: 9158139, 10634616, 11424921, 17234267; Phenotypes: Cataract 3, multiple types, MIM# 601547; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRYBB2",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:40:23.711017+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYBB1 as ready",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:40:23.702041+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crybb1 has been classified as Green List (High Evidence).",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:34:32.370111+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYBB1 were changed from to Cataract 17, multiple types, MIM# 611544",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:34:01.188896+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYBB1 were set to ",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:33:33.115544+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.305",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYBB1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:33:05.399013+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.304",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYBB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12360425, 16110300, 17460281, 21972112; Phenotypes: Cataract 17, multiple types, MIM# 611544; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:32:27.150215+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9868",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYBB1 as ready",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:32:27.141420+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9868",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crybb1 has been classified as Green List (High Evidence).",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:32:20.332901+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9868",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYBB1 were changed from to Cataract 17, multiple types, MIM# 611544",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:32:02.041363+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9867",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYBB1 were set to ",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:31:40.977780+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9866",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRYBB1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:31:22.893822+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9865",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYBB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12360425, 16110300, 17460281, 21972112; Phenotypes: Cataract 17, multiple types, MIM# 611544; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:30:27.716797+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.703",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRYBB1 as ready",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:30:27.707759+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.703",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crybb1 has been classified as Green List (High Evidence).",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:30:16.932414+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.703",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRYBB1 were changed from CATARACT 17, MULTIPLE TYPES, MONOALLELIC; CATARACT 17, MULTIPLE TYPES; CATARACT, CONGENITAL NUCLEAR, AUTOSOMAL RECESSIVE 3 to Cataract 17, multiple types, MIM# 611544",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:30:04.871871+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.702",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRYBB1 were set to ",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T17:29:50.194166+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.701",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRYBB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 12360425, 16110300, 17460281, 21972112; Phenotypes: Cataract 17, multiple types, MIM# 611544; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CRYBB1",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:38:48.616451+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9865",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFAIP3 as ready",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:38:48.602085+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9865",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfaip3 has been classified as Green List (High Evidence).",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:38:15.676891+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9865",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFAIP3 were changed from to Autoinflammatory syndrome, familial, Behcet-like, MIM# 616744; Inflammatory bowel disease",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:37:53.277078+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9864",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFAIP3 were set to ",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:37:30.297439+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9863",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNFAIP3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:37:09.641038+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9862",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNFAIP3: Rating: GREEN; Mode of pathogenicity: None; Publications: 26642243, 34030699, 33446651, 32521965, 31299923; Phenotypes: Autoinflammatory syndrome, familial, Behcet-like, MIM# 616744, Inflammatory bowel disease; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:34:52.405154+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFAIP3 as ready",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:34:52.395537+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfaip3 has been classified as Green List (High Evidence).",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:34:49.815181+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNFAIP3 were changed from to Autoinflammatory syndrome, familial, Behcet-like, MIM# 616744",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:34:25.022155+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFAIP3 were set to ",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:34:00.857516+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNFAIP3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:33:26.849894+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNFAIP3: Rating: GREEN; Mode of pathogenicity: None; Publications: 26642243; Phenotypes: Autoinflammatory syndrome, familial, Behcet-like, MIM# 616744; Mode of inheritance: None",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:27:03.967471+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNFAIP3 as ready",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:27:03.956774+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfaip3 has been classified as Green List (High Evidence).",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:26:31.929996+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNFAIP3 were set to 34030699, 33446651, 32521965, 31299923",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:25:59.386126+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TNFAIP3 as Green List (high evidence)",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T12:25:59.376747+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnfaip3 has been classified as Green List (High Evidence).",
"entity_name": "TNFAIP3",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:54:15.370932+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9862",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SFTPA1 were changed from Idiopathic pulmonary fibrosis to Idiopathic pulmonary fibrosis; Interstitial lung disease 1, MIM#\t619611",
"entity_name": "SFTPA1",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:53:56.442274+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9861",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SFTPA1: Changed phenotypes: Idiopathic pulmonary fibrosis, Interstitial lung disease 1, MIM# 619611",
"entity_name": "SFTPA1",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:53:37.230166+11:00",
"panel_name": "Pulmonary Fibrosis_Interstitial Lung Disease",
"panel_id": 162,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SFTPA1 were changed from Idiopathic pulmonary fibrosis to Idiopathic pulmonary fibrosis; Interstitial lung disease 1, MIM#\t619611",
"entity_name": "SFTPA1",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:53:02.311013+11:00",
"panel_name": "Pulmonary Fibrosis_Interstitial Lung Disease",
"panel_id": 162,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SFTPA1: Changed phenotypes: Idiopathic pulmonary fibrosis, Interstitial lung disease 1, MIM# 619611",
"entity_name": "SFTPA1",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:51:34.350563+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9861",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PI4KA were changed from Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis, MIM# 616531; Neurodevelopmental syndrome with hypomyelinating leukodystrophy to Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis, MIM# 616531; Neurodevelopmental syndrome with hypomyelinating leukodystrophy; Spastic paraplegia 84, autosomal recessive, MIM# 619621",
"entity_name": "PI4KA",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:51:01.937024+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9860",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: PI4KA: Changed phenotypes: Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis, MIM# 616531, Neurodevelopmental syndrome with hypomyelinating leukodystrophy, Spastic paraplegia 84, autosomal recessive, MIM# 619621",
"entity_name": "PI4KA",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:50:27.114220+11:00",
"panel_name": "Hereditary Spastic Paraplegia - paediatric",
"panel_id": 317,
"panel_version": "1.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PI4KA were changed from Neurodevelopmental syndrome with hypomyelinating leukodystrophy to Neurodevelopmental syndrome with hypomyelinating leukodystrophy; Spastic paraplegia 84, autosomal recessive, MIM# 619621",
"entity_name": "PI4KA",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:50:06.443189+11:00",
"panel_name": "Hereditary Spastic Paraplegia - paediatric",
"panel_id": 317,
"panel_version": "1.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PI4KA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Spastic paraplegia 84, autosomal recessive, MIM# 619621; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PI4KA",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:47:57.031721+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9860",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UCP2 as ready",
"entity_name": "UCP2",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:47:57.015561+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9860",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ucp2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UCP2",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:47:31.691466+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9860",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UCP2 were changed from to {Obesity, susceptibility to, BMIQ4} 607447; Hyperinsulinism",
"entity_name": "UCP2",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:47:12.396974+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9859",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UCP2 were set to ",
"entity_name": "UCP2",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:46:49.438196+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9858",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UCP2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "UCP2",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:46:29.149831+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9857",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UCP2 as Amber List (moderate evidence)",
"entity_name": "UCP2",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:46:29.140141+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9857",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ucp2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "UCP2",
"entity_type": "gene"
},
{
"created": "2021-11-25T11:46:12.675538+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9856",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: UCP2: Rating: AMBER; Mode of pathogenicity: None; Publications: 19065272, 11381268; Phenotypes: {Obesity, susceptibility to, BMIQ4} 607447, Hyperinsulinism; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "UCP2",
"entity_type": "gene"
}
]
}