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{
"count": 221273,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=688",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=686",
"results": [
{
"created": "2022-11-23T17:29:46.040646+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1050",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsc2 has been classified as Red List (Low Evidence).",
"entity_name": "TSC2",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:29:36.991015+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review was removed from gene: TSC2.",
"entity_name": "TSC2",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:29:27.603081+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Treatment is largely symptomatic.; to: Treatment is symptomatic.",
"entity_name": "TSC2",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:29:19.229085+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TSC2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Tuberous sclerosis-2 MIM#613254; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TSC2",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:25:02.135180+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TTC7A as Red List (low evidence)",
"entity_name": "TTC7A",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:25:02.116941+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1049",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ttc7a has been classified as Red List (Low Evidence).",
"entity_name": "TTC7A",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:24:52.503359+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review was removed from gene: TTC7A.",
"entity_name": "TTC7A",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:24:43.959573+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TTC7A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Gastrointestinal defects and immunodeficiency syndrome MIM#243150; Mode of inheritance: None",
"entity_name": "TTC7A",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:17:48.769221+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ERCC2 as Red List (low evidence)",
"entity_name": "ERCC2",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:17:48.754278+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1048",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ercc2 has been classified as Red List (Low Evidence).",
"entity_name": "ERCC2",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:17:39.264319+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review was removed from gene: ERCC2.",
"entity_name": "ERCC2",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:17:12.309610+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: ERCC2: Changed rating: RED",
"entity_name": "ERCC2",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:17:03.834169+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Bi-allelic variants in this gene cause a range of conditions, including COFS, trichothiodystrophy and XPE.\r\n\r\nDNA repair disorder.\r\n\r\nSome features are treatable: avoid exposure to UVA and UVB (found in sunlight) and UVC (found in some artificial light sources). Oral isotretinoin, oral niacinamide, topical imiquimod and topical fluorouracil.\r\n\r\nFor discussion.; to: Bi-allelic variants in this gene cause a range of conditions, including COFS, trichothiodystrophy and XPE.\r\n\r\nDNA repair disorder.\r\n\r\nSome features are treatable: avoid exposure to UVA and UVB (found in sunlight) and UVC (found in some artificial light sources). Oral isotretinoin, oral niacinamide, topical imiquimod and topical fluorouracil.\r\n",
"entity_name": "ERCC2",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:15:48.861730+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1047",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSHR were changed from Hypothyroidism, congenital, nongoitrous, 1 - MIM#275200 to Hypothyroidism, congenital, nongoitrous, 1 - MIM#275200; HYPERTHYROIDISM, FAMILIAL GESTATIONAL HYPERTHYROIDISM",
"entity_name": "TSHR",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:15:27.696148+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1046",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TSHR was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "TSHR",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:13:32.777852+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review was removed from gene: FLCN.",
"entity_name": "FLCN",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:11:52.683676+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FBN1 as Amber List (moderate evidence)",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:11:52.671738+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1045",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fbn1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:11:38.401928+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: FBN1: Changed rating: AMBER",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2022-11-23T17:04:57.857507+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag clinical trial tag was added to gene: FGFR3.",
"entity_name": "FGFR3",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:59:32.393868+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAM161A as ready",
"entity_name": "FAM161A",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:59:32.381357+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam161a has been classified as Red List (Low Evidence).",
"entity_name": "FAM161A",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:59:28.417452+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1044",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FAM161A were changed from Retinal dystrophy to Retinitis pigmentosa 28, 606068",
"entity_name": "FAM161A",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:57:56.949318+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1043",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FAM161A as Red List (low evidence)",
"entity_name": "FAM161A",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:57:56.936771+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1043",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam161a has been classified as Red List (Low Evidence).",
"entity_name": "FAM161A",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:57:45.347334+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FAM161A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Retinitis pigmentosa 28, 606068; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FAM161A",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:53:18.788874+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAM20C as ready",
"entity_name": "FAM20C",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:53:18.770367+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam20c has been classified as Red List (Low Evidence).",
"entity_name": "FAM20C",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:53:14.914063+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1042",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FAM20C were changed from Osteosclerotic bone dysplasia to Raine syndrome, MIM# 259775",
"entity_name": "FAM20C",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:53:02.862102+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1041",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FAM20C as Red List (low evidence)",
"entity_name": "FAM20C",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:53:02.837374+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1041",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam20c has been classified as Red List (Low Evidence).",
"entity_name": "FAM20C",
"entity_type": "gene"
},
{
"created": "2022-11-23T16:52:50.270301+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1040",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FAM20C: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Raine syndrome, MIM# 259775; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FAM20C",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:49:23.694342+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1803",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GPHN were set to 22040219; 11095995; 26613940; 24561070; 23393157",
"entity_name": "GPHN",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:47:55.278068+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1040",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: ACAT1.",
"entity_name": "ACAT1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:43:01.925535+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1040",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAM58A as ready",
"entity_name": "FAM58A",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:43:01.912058+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1040",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam58a has been classified as Red List (Low Evidence).",
"entity_name": "FAM58A",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:42:49.316536+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1040",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FAM58A were changed from Syndactyly - telecanthus - anogenital and renal malformations to syndactyly-telecanthus-anogenital and renal malformations syndrome MONDO:0010408",
"entity_name": "FAM58A",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:42:35.194338+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1039",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FAM58A as Red List (low evidence)",
"entity_name": "FAM58A",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:42:35.182587+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1039",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam58a has been classified as Red List (Low Evidence).",
"entity_name": "FAM58A",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:42:15.451683+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FAM58A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: syndactyly-telecanthus-anogenital and renal malformations syndrome MONDO:0010408; Mode of inheritance: Other",
"entity_name": "FAM58A",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:39:45.949694+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCA as ready",
"entity_name": "FANCA",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:39:45.937371+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fanca has been classified as Green List (High Evidence).",
"entity_name": "FANCA",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:39:42.440018+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1038",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCA were changed from Fanconi anaemia, MIM#227650 to Fanconi anaemia, complementation group A, MIM# 227650; MONDO:0009215",
"entity_name": "FANCA",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:39:24.938963+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1037",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FANCA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fanconi anaemia, complementation group A, MIM# 227650, MONDO:0009215; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCA",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:38:07.446630+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1037",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCB as ready",
"entity_name": "FANCB",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:38:07.433436+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1037",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fancb has been classified as Green List (High Evidence).",
"entity_name": "FANCB",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:38:03.906477+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1037",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCB were changed from Fanconi anaemia, MIM#300514 to Fanconi anaemia, complementation group B, MIM# 300514",
"entity_name": "FANCB",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:37:49.651857+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: FANCB.",
"entity_name": "FANCB",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:37:39.994594+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FANCB: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fanconi anaemia, complementation group B, MIM# 300514; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "FANCB",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:36:13.571046+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCC as ready",
"entity_name": "FANCC",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:36:13.558283+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fancc has been classified as Green List (High Evidence).",
"entity_name": "FANCC",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:36:10.093456+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1036",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCC were changed from Fanconi anaemia, MIM#227645 to Fanconi anemia, complementation group C, MIM# 227645; MONDO:0009213",
"entity_name": "FANCC",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:35:46.071533+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1035",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FANCC: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fanconi anemia, complementation group C, MIM# 227645 MONDO:0009213; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCC",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:34:51.361300+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1035",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCD2 as ready",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:34:51.347647+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1035",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fancd2 has been classified as Green List (High Evidence).",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:33:55.962497+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1035",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FANCD2 were changed from Fanconi anaemia, MIM#227646 to Fanconi anaemia, complementation group D2, MIM# 227646; MONDO:0009214",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:33:37.649599+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FANCD2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fanconi anaemia, complementation group D2, MIM# 227646, MONDO:0009214; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCD2",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:32:21.152732+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCG as ready",
"entity_name": "FANCG",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:32:21.140462+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fancg has been classified as Green List (High Evidence).",
"entity_name": "FANCG",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:32:13.431394+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: FANCG.",
"entity_name": "FANCG",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:32:01.995075+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FANCG: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fanconi anaemia, complementation group G, MIM# 614082, MONDO:0013565; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCG",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:31:17.135270+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FANCI as ready",
"entity_name": "FANCI",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:31:17.122224+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fanci has been classified as Green List (High Evidence).",
"entity_name": "FANCI",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:31:08.183040+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: FANCI.",
"entity_name": "FANCI",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:30:58.845044+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FANCI: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fanconi anemia, complementation group I, MIM# 609053; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCI",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:28:25.290153+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAS as ready",
"entity_name": "FAS",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:28:25.278144+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fas has been classified as Red List (Low Evidence).",
"entity_name": "FAS",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:28:20.209697+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FAS as Red List (low evidence)",
"entity_name": "FAS",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:28:20.193506+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1034",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fas has been classified as Red List (Low Evidence).",
"entity_name": "FAS",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:28:07.227040+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FAS: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Autoimmune lymphoproliferative syndrome MONDO:0017979; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "FAS",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:24:57.245808+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FBN1 as ready",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:24:57.186585+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fbn1 has been classified as Red List (Low Evidence).",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:24:53.523879+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1033",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FBN1 were changed from Marfan's syndrome; Weill-Marchesani syndrome 2, dominant; Shprintzen-Goldberg syndrome to Marfan syndrome, MIM# 154700",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:24:35.128582+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FBN1 as Red List (low evidence)",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:24:35.116789+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1032",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fbn1 has been classified as Red List (Low Evidence).",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:24:25.904492+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: FBN1.",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:24:15.137699+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FBN1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Marfan syndrome, MIM# 154700; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FBN1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:17:48.354530+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GDAP1 as ready",
"entity_name": "GDAP1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:17:48.320636+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gdap1 has been classified as Red List (Low Evidence).",
"entity_name": "GDAP1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:17:43.100389+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1031",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GDAP1 were changed from Charcot-Marie-Tooth disease to Charcot-Marie-Tooth disease, axonal, type 2K, MIM#607831; Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, MIM#607706; Charcot-Marie-Tooth disease, recessive intermediate, A, MIM#608340; Charcot-Marie-Tooth disease, type 4A, MIM#214400",
"entity_name": "GDAP1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:17:28.095341+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1030",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GDAP1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal",
"entity_name": "GDAP1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:17:19.158541+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1029",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GDAP1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "GDAP1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:17:08.478405+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1028",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GDAP1 as Red List (low evidence)",
"entity_name": "GDAP1",
"entity_type": "gene"
},
{
"created": "2022-11-23T15:17:08.465014+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1028",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gdap1 has been classified as Red List (Low Evidence).",
"entity_name": "GDAP1",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:51:35.447206+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FERMT3 as ready",
"entity_name": "FERMT3",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:51:35.431022+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fermt3 has been classified as Green List (High Evidence).",
"entity_name": "FERMT3",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:50:34.109353+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: FERMT3.",
"entity_name": "FERMT3",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:50:20.157130+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FERMT3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukocyte adhesion deficiency, type III, MIM# 612840; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FERMT3",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:46:39.742824+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGA as ready",
"entity_name": "FGA",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:46:39.729019+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fga has been classified as Green List (High Evidence).",
"entity_name": "FGA",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:46:35.954700+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1027",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FGA were changed from Afibrinogenaemia to Afibrinogenemia, congenital (MIM#202400)",
"entity_name": "FGA",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:46:18.175419+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1026",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FGA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Afibrinogenemia, congenital (MIM#202400); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FGA",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:43:54.575853+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1026",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGB as ready",
"entity_name": "FGB",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:43:54.552947+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1026",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgb has been classified as Green List (High Evidence).",
"entity_name": "FGB",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:43:51.120458+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1026",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FGB were changed from Afibrinogenaemia to Afibrinogenaemia, congenital, MIM# 202400",
"entity_name": "FGB",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:43:36.061832+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1025",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FGB: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Afibrinogenaemia, congenital, MIM# 202400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FGB",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:41:26.704010+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1025",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FGD1 as ready",
"entity_name": "FGD1",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:41:26.692565+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1025",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fgd1 has been classified as Red List (Low Evidence).",
"entity_name": "FGD1",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:41:22.321039+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1025",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FGD1 were changed from Aarskog-Scott syndrome to Aarskog-Scott syndrome, MIM # 305400; Mental retardation, X-linked syndromic 16, MIM# 305400",
"entity_name": "FGD1",
"entity_type": "gene"
},
{
"created": "2022-11-23T10:41:08.333493+11:00",
"panel_name": "gNBS",
"panel_id": 3931,
"panel_version": "0.1024",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FGD1 as Red List (low evidence)",
"entity_name": "FGD1",
"entity_type": "gene"
}
]
}