{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1072","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1070","results":[{"created":"2021-12-23T14:53:40.434163+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10352","user_name":"Lucy Spencer","item_type":"entity","text":"reviewed gene: HMGCR: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 18354102, 29480216; Phenotypes: ; Mode of inheritance: None","entity_name":"HMGCR","entity_type":"gene"},{"created":"2021-12-23T14:27:43.737395+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4390","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLVCR2 as ready","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:27:43.728227+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4390","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flvcr2 has been classified as Green List (High Evidence).","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:27:35.619750+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4390","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLVCR2 were changed from  to Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome, MIM# 225790","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:27:02.570326+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4389","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLVCR2 were set to ","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:26:15.840412+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4388","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FLVCR2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:25:30.382860+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4387","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FLVCR2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30712878, 20206334, 20518025, 20690116, 25677735; Phenotypes: Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome, MIM# 225790; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:24:10.227089+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLVCR2 as ready","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:24:10.208496+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flvcr2 has been classified as Green List (High Evidence).","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:24:07.804338+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLVCR2 were changed from  to Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome, MIM# 225790","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:23:45.295352+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLVCR2 were set to ","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:23:21.755265+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FLVCR2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:22:50.934458+11:00","panel_name":"Hydrocephalus_Ventriculomegaly","panel_id":115,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FLVCR2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30712878, 20206334, 20518025, 20690116, 25677735; Phenotypes: Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome, MIM# 225790; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:22:16.616389+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10352","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLVCR2 as ready","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:22:16.605938+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10352","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flvcr2 has been classified as Green List (High Evidence).","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:22:03.495328+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10352","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLVCR2 were changed from  to Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome, MIM# 225790","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:21:44.837345+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10351","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLVCR2 were set to ","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:21:27.082238+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10350","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FLVCR2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:21:08.785704+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10349","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FLVCR2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30712878, 20206334, 20518025, 20690116, 25677735; Phenotypes: Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome, MIM# 225790; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:20:55.988732+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1610","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLVCR2 as ready","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:20:55.972961+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1610","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flvcr2 has been classified as Green List (High Evidence).","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:20:52.036852+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1610","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLVCR2 were changed from PROLIFERATIVE VASCULOPATHY AND HYDRAENCEPHALY-HYDROCEPHALY SYNDROME to Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome, MIM# 225790","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:20:33.414109+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1609","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLVCR2 were set to ","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:19:34.134202+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1608","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FLVCR2: Added comment: The proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome is a (usually) prenatally lethal disorder characterized by hydranencephaly, a distinctive glomerular vasculopathy in the central nervous system and retina, and diffuse ischemic lesions of the brain stem, basal ganglia, and spinal cord with calcifications. It is usually diagnosed by ultrasound between 26 and 33 weeks' gestation.\r\n\r\nAt least 5 unrelated families reported.; Changed rating: GREEN; Changed publications: 30712878, 20206334, 20518025, 20690116, 25677735; Changed phenotypes: Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome, MIM# 225790","entity_name":"FLVCR2","entity_type":"gene"},{"created":"2021-12-23T14:16:17.375429+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10349","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLT4 as ready","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:16:17.366259+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10349","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flt4 has been classified as Green List (High Evidence).","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:16:06.656238+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10349","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLT4 were changed from  to Congenital heart defects, multiple types, 7, MIM# 618780; Lymphatic malformation 1, MIM# 153100","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:14:25.700791+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10348","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLT4 were set to ","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:13:38.453692+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10347","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FLT4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:13:21.080666+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10346","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FLT4: Rating: GREEN; Mode of pathogenicity: None; Publications: 9817924, 10835628, 12960217, 30232381; Phenotypes: Congenital heart defects, multiple types, 7, MIM# 618780, Lymphatic malformation 1, MIM# 153100; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:11:44.988475+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1608","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLT4 as ready","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:11:44.974594+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1608","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flt4 has been classified as Green List (High Evidence).","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:11:37.091393+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1608","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLT4 were changed from MILROY DISEASE to Congenital heart defects, multiple types, 7, MIM#\t618780; Lymphatic malformation 1, MIM# 153100","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:11:05.244216+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1607","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLT4 were set to ","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:10:49.926372+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1606","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FLT4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:10:36.600695+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1605","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FLT4: Rating: GREEN; Mode of pathogenicity: None; Publications: 9817924, 10835628, 12960217; Phenotypes: Lymphatic malformation 1, MIM# 153100; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FLT4","entity_type":"gene"},{"created":"2021-12-23T14:07:43.120584+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1605","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLNB as ready","entity_name":"FLNB","entity_type":"gene"},{"created":"2021-12-23T14:07:42.917636+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1605","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flnb has been classified as Green List (High Evidence).","entity_name":"FLNB","entity_type":"gene"},{"created":"2021-12-23T14:07:37.065881+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1605","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLNB were changed from BOOMERANG DYSPLASIA; SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; ATELOSTEOGENESIS TYPE 3; AUTOSOMAL DOMINANT LARSEN SYNDROME; ATELOSTEOGENESIS TYPE 1 to Larsen syndrome, MIM#150250; Atelosteogenesis, type I, MIM# 108720; Atelosteogenesis, type III, MIM# 108721; Boomerang dysplasia, MIM# 112310; Spondylocarpotarsal synostosis syndrome, MIM# 272460","entity_name":"FLNB","entity_type":"gene"},{"created":"2021-12-23T14:07:18.333039+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1604","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Gene associated with a number of skeletal dysplasias, ID not typically a feature.; to: Gene associated with a number of skeletal dysplasias, which are relevant to the pre-natal setting.","entity_name":"FLNB","entity_type":"gene"},{"created":"2021-12-23T14:06:58.631206+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1604","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FLNB: Changed rating: GREEN; Changed phenotypes: Larsen syndrome, MIM#150250, Atelosteogenesis, type I, MIM# 108720, Atelosteogenesis, type III, MIM# 108721, Boomerang dysplasia, MIM# 112310, Spondylocarpotarsal synostosis syndrome, MIM# 272460; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"FLNB","entity_type":"gene"},{"created":"2021-12-22T14:04:59.208464+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10346","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RNF212 were changed from Recombination rate QTL 1, MIM#612042 to Recombination rate QTL 1, MIM#612042; Spermatogenic failure 62, MIM# 619673","entity_name":"RNF212","entity_type":"gene"},{"created":"2021-12-22T14:04:36.933278+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10345","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RNF212 were set to 18239089; 29277047","entity_name":"RNF212","entity_type":"gene"},{"created":"2021-12-22T14:04:14.810919+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10344","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RNF212 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RNF212","entity_type":"gene"},{"created":"2021-12-22T14:03:56.281767+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10343","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RNF212: Rating: RED; Mode of pathogenicity: None; Publications: 31125047, 23396135; Phenotypes: Spermatogenic failure 62, MIM# 619673; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RNF212","entity_type":"gene"},{"created":"2021-12-22T13:59:16.679959+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10343","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STAG3 were changed from Premature ovarian failure 8 MIM#615723 to Premature ovarian failure 8 MIM#615723; Spermatogenic failure 61, MIM# 619672","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-22T13:58:57.959367+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10342","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STAG3 were set to 24597867; 26059840; 31803224; 31363903","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-22T13:58:33.512785+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.280","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their review","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-22T13:58:11.988189+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.280","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: STAG3: Changed phenotypes: Premature ovarian failure 8 MIM#615723","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-22T13:57:47.723120+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.280","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STAG3 were changed from Premature ovarian failure 8 MIM#615723; Spermatogenic failure 61, MIM# 619672 to Premature ovarian failure 8 MIM#615723","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-22T13:57:39.409140+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.279","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STAG3 were set to 24597867; 26059840; 31803224; 31363903; 31125047; 31682730; 32634216","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-22T13:57:16.168823+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.278","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-22T13:57:11.836333+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10341","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STAG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31125047, 31682730, 32634216; Phenotypes: Spermatogenic failure 61, MIM# 619672; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-22T13:55:46.993721+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.278","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STAG3 were changed from Premature ovarian failure 8 MIM#615723 to Premature ovarian failure 8 MIM#615723; Spermatogenic failure 61, MIM# 619672","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-22T13:55:38.373715+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.277","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STAG3 were set to 24597867; 26059840; 31803224; 31363903","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-22T13:55:14.551476+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.276","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: STAG3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-22T13:55:02.162255+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.275","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STAG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31125047, 31682730, 32634216; Phenotypes: Spermatogenic failure 61, MIM# 619672; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"STAG3","entity_type":"gene"},{"created":"2021-12-21T18:49:18.176210+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1604","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLNA as ready","entity_name":"FLNA","entity_type":"gene"},{"created":"2021-12-21T18:49:18.164212+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1604","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flna has been classified as Green List (High Evidence).","entity_name":"FLNA","entity_type":"gene"},{"created":"2021-12-21T18:49:13.307154+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1604","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLNA were changed from PERIVENTRICULAR NODULAR HETEROTOPIA TYPE 1; EPILEPTIC ENCEPHALOPATHY; FG SYNDROME TYPE 2; X-LINKED CONGENITAL IDIOPATHIC INTESTINAL PSEUDOOBSTRUCTION; MELNICK-NEEDLES SYNDROME; FRONTOMETAPHYSEAL DYSPLASIA; OTOPALATODIGITAL SYNDROME TYPE 2; TERMINAL OSSEOUS DYSPLASIA; OTOPALATODIGITAL SYNDROME TYPE 1 to Melnick-Needles syndrome, 309350; Otopalatodigital syndrome, type I 311300; Otopalatodigital syndrome, type II 304120; Terminal osseous dysplasia 300244; Heterotopia, periventricular, 1 MIM# 300049 Cardiac valvular dysplasia, X-linked MIM# 314400","entity_name":"FLNA","entity_type":"gene"},{"created":"2021-12-21T18:48:55.880804+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1603","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLNA were set to 30712878; 28425981","entity_name":"FLNA","entity_type":"gene"},{"created":"2021-12-21T18:48:40.001668+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1602","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Melnick-Needles associated with radial shortening in affected women. Male fetuses reported with absent thumbs \nSources: Expert list; to: Multiple FLNA-related disorders are relevant to this panel.\r\n\r\nMelnick-Needles associated with radial shortening in affected women. Male fetuses reported with absent thumbs \r\nSources: Expert list","entity_name":"FLNA","entity_type":"gene"},{"created":"2021-12-21T18:48:00.086242+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1602","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FLNA: Changed phenotypes: Melnick-Needles syndrome, 309350, Otopalatodigital syndrome, type I 311300, Otopalatodigital syndrome, type II 304120, Terminal osseous dysplasia 300244, Heterotopia, periventricular, 1 MIM# 300049 Cardiac valvular dysplasia, X-linked MIM# 314400","entity_name":"FLNA","entity_type":"gene"},{"created":"2021-12-21T18:45:33.554401+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1602","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FKTN as ready","entity_name":"FKTN","entity_type":"gene"},{"created":"2021-12-21T18:45:33.544412+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1602","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fktn has been classified as Green List (High Evidence).","entity_name":"FKTN","entity_type":"gene"},{"created":"2021-12-21T18:45:29.727001+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1602","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FKTN were changed from MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C4; CARDIOMYOPATHY DILATED TYPE 1X; MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITHOUT MENTAL RETARDATION TYPE B4; MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A4 to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 253800","entity_name":"FKTN","entity_type":"gene"},{"created":"2021-12-21T18:45:13.427720+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1601","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FKTN were set to ","entity_name":"FKTN","entity_type":"gene"},{"created":"2021-12-21T18:44:58.742156+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1600","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association.; to: Well established gene-disease association. Brain abnormalities are part of the more severe end of the spectrum.","entity_name":"FKTN","entity_type":"gene"},{"created":"2021-12-21T18:44:38.683934+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1600","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FKTN: Changed phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 253800","entity_name":"FKTN","entity_type":"gene"},{"created":"2021-12-21T18:16:49.375765+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1600","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FKRP as ready","entity_name":"FKRP","entity_type":"gene"},{"created":"2021-12-21T18:16:49.350015+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1600","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fkrp has been classified as Green List (High Evidence).","entity_name":"FKRP","entity_type":"gene"},{"created":"2021-12-21T18:16:45.772007+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1600","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FKRP were changed from MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES TYPE A5; MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH OR WITHOUT MENTAL RETARDATION TYPE B5; MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE TYPE C5 to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5 613153","entity_name":"FKRP","entity_type":"gene"},{"created":"2021-12-21T18:16:30.861712+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1599","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FKRP were set to ","entity_name":"FKRP","entity_type":"gene"},{"created":"2021-12-21T18:16:10.132475+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1598","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FKRP: Changed phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5 613153","entity_name":"FKRP","entity_type":"gene"},{"created":"2021-12-21T18:15:58.316141+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1598","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association.; to: Well established gene-disease association. Brain abnormalities at the more severe end of the spectrum.","entity_name":"FKRP","entity_type":"gene"},{"created":"2021-12-21T18:14:55.152799+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1598","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FH as ready","entity_name":"FH","entity_type":"gene"},{"created":"2021-12-21T18:14:55.143349+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1598","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fh has been classified as Green List (High Evidence).","entity_name":"FH","entity_type":"gene"},{"created":"2021-12-21T18:14:51.151270+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1598","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FH were changed from FUMARASE DEFICIENCY to Fumarase deficiency, MIM# 606812","entity_name":"FH","entity_type":"gene"},{"created":"2021-12-21T18:14:39.400894+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1597","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FH were set to ","entity_name":"FH","entity_type":"gene"},{"created":"2021-12-21T18:14:07.829201+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1596","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Listed as a cause of non-immune hydrops in a review, but cannot find reported cases. \nSources: Expert list; to: Listed as a cause of non-immune hydrops in a review, but cannot find reported cases.\r\n\r\nPolymicrogyria and CC abnormalities reported.\r\n\r\nSources: Expert list","entity_name":"FH","entity_type":"gene"},{"created":"2021-12-21T18:13:50.448269+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1596","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FH: Changed rating: GREEN; Changed phenotypes: Fumarase deficiency, MIM# 606812","entity_name":"FH","entity_type":"gene"},{"created":"2021-12-21T18:12:41.732496+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1596","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGFR3 as ready","entity_name":"FGFR3","entity_type":"gene"},{"created":"2021-12-21T18:12:41.722231+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1596","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr3 has been classified as Green List (High Evidence).","entity_name":"FGFR3","entity_type":"gene"},{"created":"2021-12-21T18:12:37.596742+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1596","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGFR3 were changed from CAMPTODACTYLY TALL STATURE AND HEARING LOSS SYNDROME; LACRIMO-AURICULO-DENTO-DIGITAL SYNDROME; ACHONDROPLASIA; THANATOPHORIC DYSPLASIA TYPE 2; HYPOCHONDROPLASIA; MUENKE SYNDROME; THANATOPHORIC DYSPLASIA TYPE 1; CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS to LADD syndrome, MIM#149730; Achondroplasia, MIM# 100800; Thanatophoric dysplasia, type I, MIM# 187600; Thanatophoric dysplasia, type II, MIM# 187601","entity_name":"FGFR3","entity_type":"gene"},{"created":"2021-12-21T18:12:19.729758+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1595","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGFR3 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR3","entity_type":"gene"},{"created":"2021-12-21T18:12:07.528647+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1594","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association. Variable radial ray defects (at the most severe, bilateral radial aplasia) are a feature of LADD syndrome. \nSources: Expert list; to: Well established gene-disease association with skeletal dysplasias of variable severity, including perinatal lethal. Variable radial ray defects (at the most severe, bilateral radial aplasia) are a feature of LADD syndrome. \r\nSources: Expert list","entity_name":"FGFR3","entity_type":"gene"},{"created":"2021-12-21T18:11:46.643368+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1594","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FGFR3: Changed phenotypes: LADD syndrome, MIM#149730, Achondroplasia, MIM# 100800, Thanatophoric dysplasia, type I, MIM# 187600, Thanatophoric dysplasia, type II, MIM# 187601","entity_name":"FGFR3","entity_type":"gene"},{"created":"2021-12-21T18:07:24.256701+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1594","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGFR2 as ready","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-12-21T18:07:24.246530+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1594","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr2 has been classified as Green List (High Evidence).","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-12-21T18:07:17.195231+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1594","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGFR2 were changed from JACKSON-WEISS SYNDROME; FAMILIAL SCAPHOCEPHALY SYNDROME; CROUZON SYNDROME; LACRIMO-AURICULO-DENTO-DIGITAL SYNDROME; BEARE-STEVENSON CUTIS GYRATA SYNDROME; ACROCEPHALOSYNDACTYLY TYPE V; APERT SYNDROME; ANTLEY-BIXLER SYNDROME to LADD syndrome, MIM#149730; Apert syndrome, MIM# 101200; Crouzon syndrome, MIM# 123500; Jackson-Weiss syndrome, MIM# 123150; Pfeiffer syndrome, MIM# 101600; Saethre-Chotzen syndrome, MIM# 101400","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-12-21T18:07:00.830168+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1593","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGFR2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-12-21T18:06:47.701043+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1592","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association. Radial ray abnormalities are a feature of LADD syndrome. \nSources: Expert list; to: Well established gene-disease association with multiple craniosynostosis syndromes. Radial ray abnormalities are a feature of LADD syndrome. \r\nSources: Expert list","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-12-21T18:06:25.524332+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1592","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FGFR2: Changed phenotypes: LADD syndrome, MIM#149730, Apert syndrome, MIM# 101200, Crouzon syndrome, MIM# 123500, Jackson-Weiss syndrome, MIM# 123150, Pfeiffer syndrome, MIM# 101600, Saethre-Chotzen syndrome, MIM# 101400","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-12-21T18:04:00.526235+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1592","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGFR1 as ready","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-12-21T18:04:00.506325+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1592","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr1 has been classified as Green List (High Evidence).","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-12-21T18:03:52.497766+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1592","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGFR1 were changed from Hartsfield syndrome; Encephalocraniocutaneous lipomatosis; OSTEOGLOPHONIC DYSPLASIA; KALLMANN SYNDROME TYPE 2; PFEIFFER SYNDROME; IDIOPATHIC HYPOGONADOTROPIC HYPOGONADISM to Pfeiffer syndrome, MIM# 101600","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-12-21T18:03:23.477628+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1591","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: FGFR1 was changed from  to Other","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-12-21T18:03:13.184487+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1590","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGFR1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-12-21T17:58:04.919087+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1589","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGF3 as ready","entity_name":"FGF3","entity_type":"gene"},{"created":"2021-12-21T17:58:04.903853+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.1589","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgf3 has been classified as Green List (High Evidence).","entity_name":"FGF3","entity_type":"gene"}]}