{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=654","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=652","results":[{"created":"2022-12-28T17:50:02.213914+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1700","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GJB2 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GJB2","entity_type":"gene"},{"created":"2022-12-28T17:49:51.234267+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1699","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deafness tag was added to gene: GJB2.","entity_name":"GJB2","entity_type":"gene"},{"created":"2022-12-28T17:49:41.516122+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1699","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GJB2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Deafness, autosomal recessive 1A, MIM# 220290; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GJB2","entity_type":"gene"},{"created":"2022-12-28T17:46:40.148797+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1699","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deafness tag was added to gene: GIPC3.","entity_name":"GIPC3","entity_type":"gene"},{"created":"2022-12-28T17:46:15.971434+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1699","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: GCM2.\nTag endocrine tag was added to gene: GCM2.","entity_name":"GCM2","entity_type":"gene"},{"created":"2022-12-28T17:45:55.363321+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1699","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: GCK.\nTag endocrine tag was added to gene: GCK.","entity_name":"GCK","entity_type":"gene"},{"created":"2022-12-28T17:45:32.371189+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1699","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: GCDH.","entity_name":"GCDH","entity_type":"gene"},{"created":"2022-12-28T17:45:06.587736+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1699","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: GBA.","entity_name":"GBA","entity_type":"gene"},{"created":"2022-12-28T17:44:40.141980+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1699","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GATA4 were changed from Atrial septal defect 2 MIM#607941; Atrioventricular septal defect 4 MIM#614430; Ventricular septal defect 1 MIM#614429 to Neonatal diabetes mellitus, MONDO:0016391, GATA4-related","entity_name":"GATA4","entity_type":"gene"},{"created":"2022-12-28T17:43:32.527288+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: GATA4.\nTag endocrine tag was added to gene: GATA4.","entity_name":"GATA4","entity_type":"gene"},{"created":"2022-12-28T17:43:19.743424+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Expect to be able to distinguish between the two phenotypes clinically in the newborn period.; to: Expect to be able to distinguish between the two phenotypes clinically in the newborn period.\r\n\r\nIncluded here for association with neonatal diabetes.","entity_name":"GATA4","entity_type":"gene"},{"created":"2022-12-28T17:37:55.979228+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag endocrine tag was added to gene: GATA3.\nTag deafness tag was added to gene: GATA3.","entity_name":"GATA3","entity_type":"gene"},{"created":"2022-12-28T17:37:25.421234+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag haematological tag was added to gene: GATA2.\nTag deafness tag was added to gene: GATA2.","entity_name":"GATA2","entity_type":"gene"},{"created":"2022-12-28T17:36:52.502231+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: GAMT.","entity_name":"GAMT","entity_type":"gene"},{"created":"2022-12-28T17:36:31.184266+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: GALT.","entity_name":"GALT","entity_type":"gene"},{"created":"2022-12-28T17:36:09.892301+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: GALNS.","entity_name":"GALNS","entity_type":"gene"},{"created":"2022-12-28T17:35:50.142978+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: GALK1.","entity_name":"GALK1","entity_type":"gene"},{"created":"2022-12-28T17:35:31.623069+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: GALE.","entity_name":"GALE","entity_type":"gene"},{"created":"2022-12-28T17:35:10.791641+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: GALC.","entity_name":"GALC","entity_type":"gene"},{"created":"2022-12-28T17:34:45.960911+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: GAA.","entity_name":"GAA","entity_type":"gene"},{"created":"2022-12-28T07:48:18.922212+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: G6PD.\nTag haematological tag was added to gene: G6PD.","entity_name":"G6PD","entity_type":"gene"},{"created":"2022-12-28T07:47:53.640278+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: G6PC3.","entity_name":"G6PC3","entity_type":"gene"},{"created":"2022-12-28T07:47:31.845011+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: G6PC.","entity_name":"G6PC","entity_type":"gene"},{"created":"2022-12-28T07:46:59.889186+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: FUCA1.","entity_name":"FUCA1","entity_type":"gene"},{"created":"2022-12-28T07:46:39.134623+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: FOXP3.","entity_name":"FOXP3","entity_type":"gene"},{"created":"2022-12-28T07:46:15.359523+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: FOXA2.\nTag endocrine tag was added to gene: FOXA2.","entity_name":"FOXA2","entity_type":"gene"},{"created":"2022-12-28T07:45:51.204801+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: FLAD1.","entity_name":"FLAD1","entity_type":"gene"},{"created":"2022-12-28T07:45:24.878844+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: FH.","entity_name":"FH","entity_type":"gene"},{"created":"2022-12-28T07:45:02.674522+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag haematological tag was added to gene: FGG.","entity_name":"FGG","entity_type":"gene"},{"created":"2022-12-28T07:44:42.069933+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag skeletal tag was added to gene: FGFR3.","entity_name":"FGFR3","entity_type":"gene"},{"created":"2022-12-28T07:44:19.709529+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deafness tag was added to gene: FGF3.","entity_name":"FGF3","entity_type":"gene"},{"created":"2022-12-28T07:43:56.954839+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: FGB.\nTag haematological tag was added to gene: FGB.","entity_name":"FGB","entity_type":"gene"},{"created":"2022-12-28T07:43:33.209443+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: FGA.\nTag haematological tag was added to gene: FGA.","entity_name":"FGA","entity_type":"gene"},{"created":"2022-12-28T07:43:08.027952+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: FERMT3.","entity_name":"FERMT3","entity_type":"gene"},{"created":"2022-12-28T07:42:44.653648+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: FBP1.\nTag metabolic tag was added to gene: FBP1.","entity_name":"FBP1","entity_type":"gene"},{"created":"2022-12-28T07:42:17.839058+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag haematological tag was added to gene: FANCI.","entity_name":"FANCI","entity_type":"gene"},{"created":"2022-12-28T07:41:56.792287+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag haematological tag was added to gene: FANCG.","entity_name":"FANCG","entity_type":"gene"},{"created":"2022-12-28T07:41:22.004446+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: FANCD2.\nTag haematological tag was added to gene: FANCD2.","entity_name":"FANCD2","entity_type":"gene"},{"created":"2022-12-28T07:40:58.336087+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: FANCC.\nTag haematological tag was added to gene: FANCC.","entity_name":"FANCC","entity_type":"gene"},{"created":"2022-12-28T07:40:31.179319+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag haematological tag was added to gene: FANCB.","entity_name":"FANCB","entity_type":"gene"},{"created":"2022-12-28T07:40:10.881200+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: FANCA.\nTag haematological tag was added to gene: FANCA.","entity_name":"FANCA","entity_type":"gene"},{"created":"2022-12-28T07:39:46.016884+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: FAH.","entity_name":"FAH","entity_type":"gene"},{"created":"2022-12-28T07:36:38.543675+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: F9 as ready","entity_name":"F9","entity_type":"gene"},{"created":"2022-12-28T07:36:38.530792+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: f9 has been classified as Green List (High Evidence).","entity_name":"F9","entity_type":"gene"},{"created":"2022-12-28T07:36:32.613440+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: F9.\nTag haematological tag was added to gene: F9.","entity_name":"F9","entity_type":"gene"},{"created":"2022-12-28T07:36:20.246344+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: F9: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Haemophilia B (MIM#306900); Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"F9","entity_type":"gene"},{"created":"2022-12-28T07:30:38.607088+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: F8 as ready","entity_name":"F8","entity_type":"gene"},{"created":"2022-12-28T07:30:38.593920+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: f8 has been classified as Green List (High Evidence).","entity_name":"F8","entity_type":"gene"},{"created":"2022-12-28T07:30:31.127709+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: F8.\nTag treatable tag was added to gene: F8.\nTag haematological tag was added to gene: F8.","entity_name":"F8","entity_type":"gene"},{"created":"2022-12-28T07:30:15.533069+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: F8: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Haemophilia A, MIM# 306700; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"F8","entity_type":"gene"},{"created":"2022-12-28T07:20:49.210483+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: F7 as ready","entity_name":"F7","entity_type":"gene"},{"created":"2022-12-28T07:20:49.196613+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: f7 has been classified as Green List (High Evidence).","entity_name":"F7","entity_type":"gene"},{"created":"2022-12-28T07:20:39.186462+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: F7.\nTag treatable tag was added to gene: F7.\nTag haematological tag was added to gene: F7.","entity_name":"F7","entity_type":"gene"},{"created":"2022-12-28T07:20:12.176780+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: F7: Changed rating: GREEN","entity_name":"F7","entity_type":"gene"},{"created":"2022-12-28T07:19:59.682260+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: F7: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: Factor VII deficiency, MIM# 227500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"F7","entity_type":"gene"},{"created":"2022-12-28T07:18:17.052758+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGF23 as ready","entity_name":"FGF23","entity_type":"gene"},{"created":"2022-12-28T07:18:17.040494+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgf23 has been classified as Green List (High Evidence).","entity_name":"FGF23","entity_type":"gene"},{"created":"2022-12-28T07:17:58.525041+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FGF23 as Green List (high evidence)","entity_name":"FGF23","entity_type":"gene"},{"created":"2022-12-28T07:17:58.512076+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgf23 has been classified as Green List (High Evidence).","entity_name":"FGF23","entity_type":"gene"},{"created":"2022-12-28T07:17:45.672634+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1697","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: FGF23.\nTag endocrine tag was added to gene: FGF23.","entity_name":"FGF23","entity_type":"gene"},{"created":"2022-12-28T07:17:24.356030+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1697","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FGF23 was added\ngene: FGF23 was added to gNBS. Sources: Expert list\nMode of inheritance for gene: FGF23 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: FGF23 were set to autosomal dominant hypophosphatemic rickets MONDO:0008660; familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome MONDO:0100251\nReview for gene: FGF23 was set to GREEN\nAdded comment: Mono-allelic GoF variants are associated with hypophosphataemic rickets.\r\n\r\nOnset in some is in infancy (others adolescence).\r\n\r\nTreatment: phosphate supplementation and calcitriol\r\n\r\nNon-genetic confirmatory testing:   serum phosphate, calcium, PTH, alkaline phosphatase levels, urine calcium level\r\n\r\nBi-allelic LoF variants are associated with tumoral calcinosis.\r\n\r\nAge of onset and severity are variable, but include early childhood.\r\n\r\nTreatment: dietary restriction, antacids, phosphate binders, acetazolamide, hemodialysis\r\n\r\nNon-genetic confirmatory testing:   serum phosphate, calcium, PTH, alkaline phosphatase, vitamin D serum levels, urine calcium, phosphate levels, plasma levels of the C-terminal portion of the phosphate-regulating hormone, fibroblast growth factor 23 \nSources: Expert list","entity_name":"FGF23","entity_type":"gene"},{"created":"2022-12-28T07:08:09.848258+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1696","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: F5 as ready","entity_name":"F5","entity_type":"gene"},{"created":"2022-12-28T07:08:09.836147+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1696","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: f5 has been classified as Red List (Low Evidence).","entity_name":"F5","entity_type":"gene"},{"created":"2022-12-28T07:08:05.609244+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1696","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: F5 were changed from Factor V deficiency MIM# 227400; Thrombophilia due to activated protein C resistance MIM# 188055 to Factor V deficiency, MIM# 227400 MONDO:0009210; Thrombophilia due to activated protein C resistance, MIM# 188055 MONDO:0008560; {Thrombophilia, susceptibility to, due to factor V Leiden}, MIM# 188055","entity_name":"F5","entity_type":"gene"},{"created":"2022-12-28T07:07:47.440524+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1695","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: F5 as Red List (low evidence)","entity_name":"F5","entity_type":"gene"},{"created":"2022-12-28T07:07:47.426840+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1695","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: f5 has been classified as Red List (Low Evidence).","entity_name":"F5","entity_type":"gene"},{"created":"2022-12-28T07:07:35.183386+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1694","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: F5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Factor V deficiency, MIM# 227400 MONDO:0009210, Thrombophilia due to activated protein C resistance, MIM# 188055 MONDO:0008560, {Thrombophilia, susceptibility to, due to factor V Leiden}, MIM# 188055; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"F5","entity_type":"gene"},{"created":"2022-12-28T07:05:34.782836+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1694","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: F2 as ready","entity_name":"F2","entity_type":"gene"},{"created":"2022-12-28T07:05:34.770683+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1694","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: f2 has been classified as Red List (Low Evidence).","entity_name":"F2","entity_type":"gene"},{"created":"2022-12-28T07:05:30.794325+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1694","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: F2 were changed from Prothrombin deficiency, MIM#613679 to Dysprothrombinemia MIM#613679; Hypoprothrombinemia MIM#613679; Thrombophilia due to thrombin defect MIM#188050","entity_name":"F2","entity_type":"gene"},{"created":"2022-12-28T07:05:15.410667+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1693","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: F2 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"F2","entity_type":"gene"},{"created":"2022-12-28T07:05:00.212305+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1692","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: F2 as Red List (low evidence)","entity_name":"F2","entity_type":"gene"},{"created":"2022-12-28T07:05:00.197696+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1692","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: f2 has been classified as Red List (Low Evidence).","entity_name":"F2","entity_type":"gene"},{"created":"2022-12-28T07:04:48.708621+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1691","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: F2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Dysprothrombinemia MIM#613679, Hypoprothrombinemia MIM#613679, Thrombophilia due to thrombin defect MIM#188050; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"F2","entity_type":"gene"},{"created":"2022-12-28T06:59:31.916142+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1691","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: F13A1 as ready","entity_name":"F13A1","entity_type":"gene"},{"created":"2022-12-28T06:59:31.903610+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1691","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: f13a1 has been classified as Green List (High Evidence).","entity_name":"F13A1","entity_type":"gene"},{"created":"2022-12-28T06:59:25.103317+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1691","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: F13A1.\nTag haematological tag was added to gene: F13A1.","entity_name":"F13A1","entity_type":"gene"},{"created":"2022-12-28T06:59:11.017154+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1691","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: F13A1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Factor XIIIA deficiency, MIM# 613225; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"F13A1","entity_type":"gene"},{"created":"2022-12-28T06:55:51.691335+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1691","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: F11 as ready","entity_name":"F11","entity_type":"gene"},{"created":"2022-12-28T06:55:51.671648+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1691","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: f11 has been classified as Red List (Low Evidence).","entity_name":"F11","entity_type":"gene"},{"created":"2022-12-28T06:55:47.615940+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1691","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: F11 were changed from Factor XI deficiency to Factor XI deficiency, autosomal dominant 612416; Factor XI deficiency, autosomal recessive, MIM#612416","entity_name":"F11","entity_type":"gene"},{"created":"2022-12-28T06:55:33.788358+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1690","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: F11 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"F11","entity_type":"gene"},{"created":"2022-12-28T06:55:19.524960+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1689","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: F11 as Red List (low evidence)","entity_name":"F11","entity_type":"gene"},{"created":"2022-12-28T06:55:19.505138+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1689","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: f11 has been classified as Red List (Low Evidence).","entity_name":"F11","entity_type":"gene"},{"created":"2022-12-28T06:55:07.513558+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: F11: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Factor XI deficiency, autosomal dominant 612416, Factor XI deficiency, autosomal recessive, MIM#612416; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"F11","entity_type":"gene"},{"created":"2022-12-27T19:45:36.126468+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: ETHE1.","entity_name":"ETHE1","entity_type":"gene"},{"created":"2022-12-27T19:45:09.581118+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: ETFDH.","entity_name":"ETFDH","entity_type":"gene"},{"created":"2022-12-27T19:44:22.622646+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: ETFB.\nTag metabolic tag was added to gene: ETFB.","entity_name":"ETFB","entity_type":"gene"},{"created":"2022-12-27T19:43:53.568462+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: ETFA.","entity_name":"ETFA","entity_type":"gene"},{"created":"2022-12-27T19:43:19.571757+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deafness tag was added to gene: ESRRB.","entity_name":"ESRRB","entity_type":"gene"},{"created":"2022-12-27T19:42:56.199902+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deafness tag was added to gene: ESPN.","entity_name":"ESPN","entity_type":"gene"},{"created":"2022-12-27T19:42:26.893583+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deafness tag was added to gene: EPS8.","entity_name":"EPS8","entity_type":"gene"},{"created":"2022-12-27T19:41:59.470939+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag endocrine tag was added to gene: ENPP1.\nTag vascular tag was added to gene: ENPP1.","entity_name":"ENPP1","entity_type":"gene"},{"created":"2022-12-27T19:41:15.780448+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: ENG.\nTag vascular tag was added to gene: ENG.","entity_name":"ENG","entity_type":"gene"},{"created":"2022-12-27T19:40:47.225424+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: ELANE.\nTag immunological tag was added to gene: ELANE.","entity_name":"ELANE","entity_type":"gene"},{"created":"2022-12-27T19:40:23.792422+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: EIF2AK3.\nTag endocrine tag was added to gene: EIF2AK3.","entity_name":"EIF2AK3","entity_type":"gene"},{"created":"2022-12-27T19:39:40.961292+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag gastrointestinal tag was added to gene: EFL1.","entity_name":"EFL1","entity_type":"gene"},{"created":"2022-12-27T19:39:15.557183+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deafness tag was added to gene: EDNRB.","entity_name":"EDNRB","entity_type":"gene"},{"created":"2022-12-27T19:38:54.759432+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deafness tag was added to gene: EDN3.","entity_name":"EDN3","entity_type":"gene"},{"created":"2022-12-27T19:38:33.396687+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Tag endocrine tag was added to gene: DUOXA2.","entity_name":"DUOXA2","entity_type":"gene"}]}