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{
"count": 221304,
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"results": [
{
"created": "2020-04-10T18:13:57.094056+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2093",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IL21 were set to ",
"entity_name": "IL21",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:13:43.250626+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2092",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL21 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL21",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:13:21.323084+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2091",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IL21 as Red List (low evidence)",
"entity_name": "IL21",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:13:21.310045+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2091",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il21 has been classified as Red List (Low Evidence).",
"entity_name": "IL21",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:13:14.570986+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IL21 were set to ",
"entity_name": "IL21",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:13:01.605086+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2090",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IL21: Rating: RED; Mode of pathogenicity: None; Publications: 24746753; Phenotypes: Immunodeficiency, common variable, 11, MIM# 615767; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL21",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:12:50.960366+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL21 was changed from Unknown to Unknown",
"entity_name": "IL21",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:12:13.456919+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IL21 as Red List (low evidence)",
"entity_name": "IL21",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:12:13.447758+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il21 has been classified as Red List (Low Evidence).",
"entity_name": "IL21",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:11:41.893949+10:00",
"panel_name": "Combined Immunodeficiency",
"panel_id": 223,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IL21: Rating: RED; Mode of pathogenicity: None; Publications: 24746753; Phenotypes: Immunodeficiency, common variable, 11, MIM# 615767; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL21",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:07:21.503607+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2090",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL17F as ready",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:07:21.494694+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2090",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il17f has been classified as Red List (Low Evidence).",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:07:10.482163+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2090",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IL17F were changed from to Candidiasis, familial, 6, autosomal dominant, MIM# 613956",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:06:49.783175+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2089",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IL17F were set to ",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:06:28.006616+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2088",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL17F was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:06:08.609456+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2087",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IL17F as Red List (low evidence)",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:06:08.600294+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2087",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il17f has been classified as Red List (Low Evidence).",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:05:48.646102+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2086",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IL17F: Rating: RED; Mode of pathogenicity: None; Publications: 21350122; Phenotypes: Candidiasis, familial, 6, autosomal dominant, MIM# 613956; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:03:20.936039+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.29",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IL17F were changed from to Candidiasis, familial, 6, autosomal dominant, MIM# 613956",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:02:55.511986+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IL17F were set to ",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:02:31.850221+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL17F was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:02:07.904011+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IL17F as Red List (low evidence)",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T18:02:07.894690+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il17f has been classified as Red List (Low Evidence).",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:59:59.784157+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IL17F: Rating: RED; Mode of pathogenicity: None; Publications: 21350122; Phenotypes: Candidiasis, familial, 6, autosomal dominant, MIM# 613956; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "IL17F",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:35:05.112175+10:00",
"panel_name": "Phagocyte Defects",
"panel_id": 233,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FPR1 as ready",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:35:05.102588+10:00",
"panel_name": "Phagocyte Defects",
"panel_id": 233,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fpr1 has been classified as Red List (Low Evidence).",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:35:02.719514+10:00",
"panel_name": "Phagocyte Defects",
"panel_id": 233,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FPR1 were changed from to Periodontitis",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:34:39.687950+10:00",
"panel_name": "Phagocyte Defects",
"panel_id": 233,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FPR1 were set to ",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:34:15.189235+10:00",
"panel_name": "Phagocyte Defects",
"panel_id": 233,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FPR1 as Red List (low evidence)",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:34:15.176474+10:00",
"panel_name": "Phagocyte Defects",
"panel_id": 233,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fpr1 has been classified as Red List (Low Evidence).",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:33:37.356408+10:00",
"panel_name": "Phagocyte Defects",
"panel_id": 233,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FPR1: Rating: RED; Mode of pathogenicity: None; Publications: 29105764, 28371599; Phenotypes: Periodontitis; Mode of inheritance: None",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:32:56.305750+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2086",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FPR1 as ready",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:32:56.297032+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2086",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fpr1 has been classified as Red List (Low Evidence).",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:32:48.784168+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2086",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FPR1 were changed from to Periodontitis",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:32:28.530744+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2085",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FPR1 were set to ",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:32:14.396657+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2084",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FPR1 as Red List (low evidence)",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:32:14.387788+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2084",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fpr1 has been classified as Red List (Low Evidence).",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:31:55.021899+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2083",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FPR1: Rating: RED; Mode of pathogenicity: None; Publications: 29105764, 28371599; Phenotypes: Periodontitis; Mode of inheritance: None",
"entity_name": "FPR1",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:22:11.649059+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2083",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FCN3 as ready",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:22:11.636271+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2083",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fcn3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:22:04.060708+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2083",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FCN3 were changed from to Immunodeficiency due to ficolin 3 deficiency, MIM# 613860",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:21:48.830776+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2082",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FCN3 were set to ",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:21:34.389981+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2081",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FCN3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:21:20.714701+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2080",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FCN3 as Amber List (moderate evidence)",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:21:20.701496+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2080",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fcn3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:21:01.987010+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2079",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FCN3: Rating: AMBER; Mode of pathogenicity: None; Publications: 25662573, 22226667, 19535802, 20971976; Phenotypes: Immunodeficiency due to ficolin 3 deficiency, MIM# 613860; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:19:39.840202+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FCN3 as ready",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:19:39.824589+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fcn3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:19:37.281042+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FCN3 were changed from to Immunodeficiency due to ficolin 3 deficiency, MIM# 613860",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:19:14.057090+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FCN3 were set to ",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:18:49.428379+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FCN3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:18:25.819464+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FCN3 as Amber List (moderate evidence)",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:18:25.811552+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fcn3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:17:54.404321+10:00",
"panel_name": "Complement Deficiencies",
"panel_id": 224,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FCN3: Rating: AMBER; Mode of pathogenicity: None; Publications: 25662573, 22226667, 19535802, 20971976; Phenotypes: Immunodeficiency due to ficolin 3 deficiency, MIM# 613860; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FCN3",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:10:14.868432+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2079",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FCGR3A as ready",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:10:14.855084+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2079",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fcgr3a has been classified as Amber List (Moderate Evidence).",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:10:05.417188+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2079",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FCGR3A were changed from to Immunodeficiency 20, MIM# 615707",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:09:46.347633+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2078",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FCGR3A were set to ",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:09:26.916649+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2077",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FCGR3A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:09:08.439290+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2076",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FCGR3A as Amber List (moderate evidence)",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:09:08.425128+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2076",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fcgr3a has been classified as Amber List (Moderate Evidence).",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:08:39.652584+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2075",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FCGR3A: Rating: AMBER; Mode of pathogenicity: None; Publications: 8874200, 23006327, 8608639; Phenotypes: Immunodeficiency 20, MIM# 615707; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:07:55.483515+10:00",
"panel_name": "Susceptibility to Viral Infections",
"panel_id": 237,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FCGR3A as ready",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:07:55.475223+10:00",
"panel_name": "Susceptibility to Viral Infections",
"panel_id": 237,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fcgr3a has been classified as Amber List (Moderate Evidence).",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:07:52.110776+10:00",
"panel_name": "Susceptibility to Viral Infections",
"panel_id": 237,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FCGR3A were changed from to Immunodeficiency 20, MIM# 615707",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:07:28.230303+10:00",
"panel_name": "Susceptibility to Viral Infections",
"panel_id": 237,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FCGR3A were set to ",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:06:58.278494+10:00",
"panel_name": "Susceptibility to Viral Infections",
"panel_id": 237,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FCGR3A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:06:34.589782+10:00",
"panel_name": "Susceptibility to Viral Infections",
"panel_id": 237,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FCGR3A as Amber List (moderate evidence)",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:06:34.576647+10:00",
"panel_name": "Susceptibility to Viral Infections",
"panel_id": 237,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fcgr3a has been classified as Amber List (Moderate Evidence).",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:03:59.557908+10:00",
"panel_name": "Susceptibility to Viral Infections",
"panel_id": 237,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FCGR3A: Rating: AMBER; Mode of pathogenicity: None; Publications: 8874200, 23006327, 8608639; Phenotypes: Immunodeficiency 20, MIM# 615707; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:03:08.710034+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FCGR3A as ready",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:03:08.696584+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fcgr3a has been classified as Amber List (Moderate Evidence).",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:03:06.339319+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FCGR3A were changed from to Immunodeficiency 20, MIM# 615707",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:02:39.615761+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FCGR3A were set to ",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:02:09.346468+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FCGR3A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:01:23.424928+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FCGR3A as Amber List (moderate evidence)",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T17:01:23.415678+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fcgr3a has been classified as Amber List (Moderate Evidence).",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:53:23.810763+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FCGR3A: Rating: AMBER; Mode of pathogenicity: None; Publications: 8874200, 23006327, 8608639; Phenotypes: Immunodeficiency 20, MIM# 615707; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FCGR3A",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:34:51.578247+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EPCAM as ready",
"entity_name": "EPCAM",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:34:51.569095+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: epcam has been classified as Amber List (Moderate Evidence).",
"entity_name": "EPCAM",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:34:45.501008+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EPCAM were changed from to Diarrhea 5, with tufting enteropathy, congenital, MIM# 613217",
"entity_name": "EPCAM",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:34:19.304432+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EPCAM were set to ",
"entity_name": "EPCAM",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:33:54.701242+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EPCAM was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EPCAM",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:33:31.375481+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EPCAM as Amber List (moderate evidence)",
"entity_name": "EPCAM",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:33:31.362657+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: epcam has been classified as Amber List (Moderate Evidence).",
"entity_name": "EPCAM",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:33:02.437891+10:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EPCAM: Rating: AMBER; Mode of pathogenicity: None; Publications: 27302973; Phenotypes: Diarrhea 5, with tufting enteropathy, congenital, MIM# 613217; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EPCAM",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:07:33.683104+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CR2 as ready",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:07:33.673962+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cr2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:07:30.625956+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CR2 were changed from to Immunodeficiency, common variable, 7, MIM# 614699",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:06:58.819111+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CR2 were set to ",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:06:34.850545+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CR2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:06:10.969371+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CR2 as Amber List (moderate evidence)",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:06:10.949083+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cr2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:05:40.534992+10:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CR2: Rating: AMBER; Mode of pathogenicity: None; Publications: 22035880, 26325596; Phenotypes: Immunodeficiency, common variable, 7, MIM# 614699; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:04:59.910015+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2075",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CR2 as ready",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:04:59.901137+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2075",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cr2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:04:51.580204+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2075",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CR2 were set to ",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:04:21.907956+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2074",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CR2 were changed from to Immunodeficiency, common variable, 7, MIM# 614699",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:03:59.031588+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.2073",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CR2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CR2",
"entity_type": "gene"
},
{
"created": "2020-04-10T16:03:55.278487+10:00",
"panel_name": "Dilated Cardiomyopathy",
"panel_id": 95,
"panel_version": "0.25",
"user_name": "Crystle Lee",
"item_type": "entity",
"text": "reviewed gene: DMD: Rating: GREEN; Mode of pathogenicity: None; Publications: 26066469; Phenotypes: Cardiomyopathy, dilated, 3B (MIM#302045); Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "DMD",
"entity_type": "gene"
}
]
}