{"count":220403,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=953","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=951","results":[{"created":"2022-03-03T09:51:24.547487+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4670","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcyt2 has been classified as Red List (Low Evidence).","entity_name":"PCYT2","entity_type":"gene"},{"created":"2022-03-03T09:51:18.673452+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4670","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PCYT2 as Red List (low evidence)","entity_name":"PCYT2","entity_type":"gene"},{"created":"2022-03-03T09:51:18.662364+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4670","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcyt2 has been classified as Red List (Low Evidence).","entity_name":"PCYT2","entity_type":"gene"},{"created":"2022-03-03T09:50:46.624706+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4669","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: ACTC1 were changed from Atrial septal defect 5 612794; Cardiomyopathy, hypertrophic, 11 612098 to Atrial septal defect 5, MIM# 612794; Cardiomyopathy, hypertrophic, 11 MIM# 612098","entity_name":"ACTC1","entity_type":"gene"},{"created":"2022-03-03T09:50:42.190778+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4668","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCDH12 as ready","entity_name":"PCDH12","entity_type":"gene"},{"created":"2022-03-03T09:50:42.180667+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4668","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcdh12 has been classified as Green List (High Evidence).","entity_name":"PCDH12","entity_type":"gene"},{"created":"2022-03-03T09:50:36.675647+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4668","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PCDH12 as Green List (high evidence)","entity_name":"PCDH12","entity_type":"gene"},{"created":"2022-03-03T09:50:36.663565+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4668","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcdh12 has been classified as Green List (High Evidence).","entity_name":"PCDH12","entity_type":"gene"},{"created":"2022-03-03T09:49:34.627544+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4667","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PARP6 as ready","entity_name":"PARP6","entity_type":"gene"},{"created":"2022-03-03T09:49:34.614241+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4667","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: parp6 has been classified as Green List (High Evidence).","entity_name":"PARP6","entity_type":"gene"},{"created":"2022-03-03T09:48:23.815272+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4667","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PARP6 as Green List (high evidence)","entity_name":"PARP6","entity_type":"gene"},{"created":"2022-03-03T09:48:23.802630+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4667","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: parp6 has been classified as Green List (High Evidence).","entity_name":"PARP6","entity_type":"gene"},{"created":"2022-03-03T09:45:57.452331+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4666","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NKX2-5 as ready","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2022-03-03T09:45:57.442727+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4666","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nkx2-5 has been classified as Green List (High Evidence).","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2022-03-03T09:45:48.160900+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4666","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: NKX2-5 as ready","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2022-03-03T09:45:48.151042+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4666","user_name":"Alison Yeung","item_type":"entity","text":"Gene: nkx2-5 has been classified as Green List (High Evidence).","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2022-03-03T09:44:45.280323+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4666","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: NKX2-5 were changed from CONGENITAL HYPOTHYROIDISM NON-GOITROUS TYPE 5; TETRALOGY OF FALLOT; ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS to Atrial septal defect 7, with or without AV conduction defects, MIM# 108900; Hypoplastic left heart syndrome 2, MIM# 614435; Tetralogy of Fallot, MIM# 187500; Ventricular septal defect 3, MIM# \t614432; Hypothyroidism, congenital nongoitrous, 5, MIM# 225250","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2022-03-03T09:44:39.721876+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4665","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NPC2 as ready","entity_name":"NPC2","entity_type":"gene"},{"created":"2022-03-03T09:44:39.711576+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4665","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: npc2 has been classified as Amber List (Moderate Evidence).","entity_name":"NPC2","entity_type":"gene"},{"created":"2022-03-03T09:44:35.937589+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4665","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NPC2 were changed from NIEMANN-PICK DISEASE, TYPE C2 to Niemann-pick disease, type C2, MIM# 607625","entity_name":"NPC2","entity_type":"gene"},{"created":"2022-03-03T09:44:21.997515+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4664","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NPC2 were set to ","entity_name":"NPC2","entity_type":"gene"},{"created":"2022-03-03T09:44:09.009067+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4663","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NPC2 as Amber List (moderate evidence)","entity_name":"NPC2","entity_type":"gene"},{"created":"2022-03-03T09:44:08.995864+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4663","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: npc2 has been classified as Amber List (Moderate Evidence).","entity_name":"NPC2","entity_type":"gene"},{"created":"2022-03-03T09:43:53.870545+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4662","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: NPC2: Changed rating: AMBER","entity_name":"NPC2","entity_type":"gene"},{"created":"2022-03-03T09:42:07.715908+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4662","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NPHP1 as ready","entity_name":"NPHP1","entity_type":"gene"},{"created":"2022-03-03T09:42:07.697478+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4662","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nphp1 has been classified as Green List (High Evidence).","entity_name":"NPHP1","entity_type":"gene"},{"created":"2022-03-03T09:42:03.689495+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4662","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NPHP1 were changed from NEPHRONOPHTHISIS TYPE 1; JOUBERT SYNDROME TYPE 4; SENIOR-LOKEN SYNDROME TYPE 1 to Joubert syndrome 4, MIM# 609583","entity_name":"NPHP1","entity_type":"gene"},{"created":"2022-03-03T09:41:50.350087+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4661","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NPHP1 were set to ","entity_name":"NPHP1","entity_type":"gene"},{"created":"2022-03-03T09:41:43.744315+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4660","user_name":"Alison Yeung","item_type":"entity","text":"Publications for gene: NKX2-5 were set to ","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2022-03-03T09:41:28.721605+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4659","user_name":"Alison Yeung","item_type":"entity","text":"Mode of inheritance for gene: NKX2-5 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NKX2-5","entity_type":"gene"},{"created":"2022-03-03T09:40:17.468552+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4658","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NPHP3 as ready","entity_name":"NPHP3","entity_type":"gene"},{"created":"2022-03-03T09:40:17.453760+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4658","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nphp3 has been classified as Green List (High Evidence).","entity_name":"NPHP3","entity_type":"gene"},{"created":"2022-03-03T09:40:08.777141+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4658","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NPHP3 were changed from RENAL-HEPATIC-PANCREATIC DYSPLASIA; NEPHRONOPHTHISIS TYPE 3; MECKEL SYNDROME TYPE 7 to Meckel syndrome 7, MIM# 267010; Nephronophthisis 3, MIM# 604387; Renal-hepatic-pancreatic dysplasia 1, MIM# 208540","entity_name":"NPHP3","entity_type":"gene"},{"created":"2022-03-03T09:39:58.502623+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4657","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NPHP3 were set to ","entity_name":"NPHP3","entity_type":"gene"},{"created":"2022-03-03T09:39:42.665669+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4656","user_name":"Alison Yeung","item_type":"entity","text":"Marked gene: NIPBL as ready","entity_name":"NIPBL","entity_type":"gene"},{"created":"2022-03-03T09:39:42.652529+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4656","user_name":"Alison Yeung","item_type":"entity","text":"Gene: nipbl has been classified as Green List (High Evidence).","entity_name":"NIPBL","entity_type":"gene"},{"created":"2022-03-03T09:39:38.459001+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4656","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: NPHP3: Changed phenotypes: Meckel syndrome 7, MIM# 267010, Nephronophthisis 3, MIM# 604387, Renal-hepatic-pancreatic dysplasia 1, MIM# 208540","entity_name":"NPHP3","entity_type":"gene"},{"created":"2022-03-03T09:39:37.862712+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4656","user_name":"Alison Yeung","item_type":"entity","text":"Phenotypes for gene: NIPBL were changed from CORNELIA DE LANGE SYNDROME TYPE 1 to Cornelia de Lange syndrome 1, MIM# 122470","entity_name":"NIPBL","entity_type":"gene"},{"created":"2022-03-03T09:39:16.322911+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4655","user_name":"Alison Yeung","item_type":"entity","text":"Mode of inheritance for gene: NIPBL was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NIPBL","entity_type":"gene"},{"created":"2022-03-03T09:39:04.365499+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4654","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: NPHP3: Changed rating: GREEN","entity_name":"NPHP3","entity_type":"gene"},{"created":"2022-03-03T09:38:53.945172+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4654","user_name":"Alison Yeung","item_type":"entity","text":"reviewed gene: NIPBL: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cornelia de Lange syndrome 1, MIM# 122470; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NIPBL","entity_type":"gene"},{"created":"2022-03-03T09:33:19.405290+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4654","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NPHP4 as ready","entity_name":"NPHP4","entity_type":"gene"},{"created":"2022-03-03T09:33:19.394182+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4654","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nphp4 has been classified as Green List (High Evidence).","entity_name":"NPHP4","entity_type":"gene"},{"created":"2022-03-03T09:33:13.594606+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4654","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NPHP4 were changed from NEPHRONOPHTHISIS TYPE 4 to Nephronophthisis 4, MIM# 606966; Senior-Loken syndrome 4, MIM# 606996","entity_name":"NPHP4","entity_type":"gene"},{"created":"2022-03-03T09:33:01.419961+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4653","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NPHP4 were set to ","entity_name":"NPHP4","entity_type":"gene"},{"created":"2022-03-03T09:31:40.718834+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4652","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NRAS as ready","entity_name":"NRAS","entity_type":"gene"},{"created":"2022-03-03T09:31:40.698535+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4652","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nras has been classified as Green List (High Evidence).","entity_name":"NRAS","entity_type":"gene"},{"created":"2022-03-03T09:31:24.617080+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4652","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NRAS were changed from NOONAN SYNDROME TYPE 6 to Noonan syndrome 6, MIM# 613224","entity_name":"NRAS","entity_type":"gene"},{"created":"2022-03-03T09:31:11.800327+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4651","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NRAS were set to ","entity_name":"NRAS","entity_type":"gene"},{"created":"2022-03-03T09:30:58.821902+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4650","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: NRAS was changed from  to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"NRAS","entity_type":"gene"},{"created":"2022-03-03T09:30:47.644418+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4649","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NRAS was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NRAS","entity_type":"gene"},{"created":"2022-03-03T09:29:29.751262+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4648","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NSD1 as ready","entity_name":"NSD1","entity_type":"gene"},{"created":"2022-03-03T09:29:29.737977+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4648","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nsd1 has been classified as Green List (High Evidence).","entity_name":"NSD1","entity_type":"gene"},{"created":"2022-03-03T09:29:25.794176+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4648","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NSD1 were changed from BECKWITH-WIEDEMANN SYNDROME; WEAVER SYNDROME; SOTOS SYNDROME to Sotos syndrome 1, MIM# 117550","entity_name":"NSD1","entity_type":"gene"},{"created":"2022-03-03T09:29:13.265715+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4647","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NSD1 were set to ","entity_name":"NSD1","entity_type":"gene"},{"created":"2022-03-03T09:29:02.453535+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4646","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NSD1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NSD1","entity_type":"gene"},{"created":"2022-03-03T09:28:48.572148+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4645","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"NSD1","entity_type":"gene"},{"created":"2022-03-03T09:28:44.664789+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4645","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: NSD1: Overgrowth, congenital anomalies.","entity_name":"NSD1","entity_type":"gene"},{"created":"2022-03-03T09:28:30.854392+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4645","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: NSD1: Changed rating: GREEN","entity_name":"NSD1","entity_type":"gene"},{"created":"2022-03-03T09:27:34.698475+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4645","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NSDHL as ready","entity_name":"NSDHL","entity_type":"gene"},{"created":"2022-03-03T09:27:34.688822+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4645","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nsdhl has been classified as Green List (High Evidence).","entity_name":"NSDHL","entity_type":"gene"},{"created":"2022-03-03T09:27:31.009636+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4645","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NSDHL were changed from CK SYNDROME; CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS to CK syndrome , MIM#300831","entity_name":"NSDHL","entity_type":"gene"},{"created":"2022-03-03T09:27:16.559292+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4644","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NSDHL were set to ","entity_name":"NSDHL","entity_type":"gene"},{"created":"2022-03-03T09:25:32.450030+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4643","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NSDHL was changed from X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"NSDHL","entity_type":"gene"},{"created":"2022-03-03T09:25:17.099050+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4642","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NSDHL: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: CK syndrome , MIM#300831; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"NSDHL","entity_type":"gene"},{"created":"2022-03-03T09:24:01.267825+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4642","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NUP107 as ready","entity_name":"NUP107","entity_type":"gene"},{"created":"2022-03-03T09:24:01.250363+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4642","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nup107 has been classified as Green List (High Evidence).","entity_name":"NUP107","entity_type":"gene"},{"created":"2022-03-03T09:23:33.939803+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4642","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NUP107 were changed from EARLY-CHILDHOOD-ONSET STEROID-RESISTANT NEPHROTIC SYNDROME to Galloway-Mowat syndrome 7, MIM# 618348","entity_name":"NUP107","entity_type":"gene"},{"created":"2022-03-03T09:23:21.586406+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4641","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NUP107 were set to ","entity_name":"NUP107","entity_type":"gene"},{"created":"2022-03-03T09:22:46.835335+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4640","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OCRL as ready","entity_name":"OCRL","entity_type":"gene"},{"created":"2022-03-03T09:22:46.825962+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4640","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ocrl has been classified as Green List (High Evidence).","entity_name":"OCRL","entity_type":"gene"},{"created":"2022-03-03T09:21:41.076527+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4640","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OFD1 as ready","entity_name":"OFD1","entity_type":"gene"},{"created":"2022-03-03T09:21:41.065403+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4640","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ofd1 has been classified as Green List (High Evidence).","entity_name":"OFD1","entity_type":"gene"},{"created":"2022-03-03T09:21:37.123159+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4640","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OFD1 were changed from SIMPSON-GOLABI-BEHMEL SYNDROME TYPE 2; JOUBERT SYNDROME TYPE 10; ORAL-FACIAL-DIGITAL SYNDROME TYPE 1 to Orofaciodigital syndrome I, MIM# 311200; Joubert syndrome 10, MIM# 300804","entity_name":"OFD1","entity_type":"gene"},{"created":"2022-03-03T09:21:18.645610+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4639","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: XLD. Polydactyly is a rare feature. Primarily facial/neurological features.; to: Well established gene-disease associations, multiple congenital anomalies.","entity_name":"OFD1","entity_type":"gene"},{"created":"2022-03-03T09:21:01.715864+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4639","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: OFD1: Changed phenotypes: Orofaciodigital syndrome I, MIM# 311200, Joubert syndrome 10, MIM# 300804","entity_name":"OFD1","entity_type":"gene"},{"created":"2022-03-03T09:20:53.559946+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4639","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: OFD1: Changed rating: GREEN; Changed phenotypes: Orofaciodigital syndrome I, MIM# 311200, Joubert syndrome 10 300804; Changed mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"OFD1","entity_type":"gene"},{"created":"2022-03-03T09:19:16.251948+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4639","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCGF2 as ready","entity_name":"PCGF2","entity_type":"gene"},{"created":"2022-03-03T09:19:16.242839+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4639","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcgf2 has been classified as Green List (High Evidence).","entity_name":"PCGF2","entity_type":"gene"},{"created":"2022-03-03T09:19:12.494975+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4639","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCGF2 were changed from Craniofacial Neurological Cardiovascular and Skeletal Features; Intellectual disability; INTELLECTUAL DUSBILITY to Turnpenny-Fry syndrome, MIM# 618371","entity_name":"PCGF2","entity_type":"gene"},{"created":"2022-03-03T09:18:58.701830+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4638","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PCGF2 were set to 30526864","entity_name":"PCGF2","entity_type":"gene"},{"created":"2022-03-03T09:18:43.249698+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4637","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PCGF2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PCGF2","entity_type":"gene"},{"created":"2022-03-03T09:15:59.007064+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4636","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCNT as ready","entity_name":"PCNT","entity_type":"gene"},{"created":"2022-03-03T09:15:58.995088+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4636","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcnt has been classified as Green List (High Evidence).","entity_name":"PCNT","entity_type":"gene"},{"created":"2022-03-03T09:15:55.451670+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4636","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCNT were changed from MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II to Microcephalic osteodysplastic primordial dwarfism, type II, MIM# 210720; MONDO:0008872","entity_name":"PCNT","entity_type":"gene"},{"created":"2022-03-03T09:15:42.254566+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4635","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PCNT were set to ","entity_name":"PCNT","entity_type":"gene"},{"created":"2022-03-03T09:14:53.887724+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4634","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDHA1 as ready","entity_name":"PDHA1","entity_type":"gene"},{"created":"2022-03-03T09:14:53.877778+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4634","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pdha1 has been classified as Green List (High Evidence).","entity_name":"PDHA1","entity_type":"gene"},{"created":"2022-03-03T09:14:50.051631+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4634","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDHA1 were changed from X-LINKED LEIGH SYNDROME; PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY IN FEMALES; INTELLECTUAL DISABILTIY; Pyruvate dehydrogenase E1-alpha deficiency to Pyruvate dehydrogenase E1-alpha deficiency, MIM# 312170","entity_name":"PDHA1","entity_type":"gene"},{"created":"2022-03-03T09:14:37.226583+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4633","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDHA1 were set to 26865159","entity_name":"PDHA1","entity_type":"gene"},{"created":"2022-03-03T09:14:20.739925+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4632","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Variants in this gene can cause congenital anomalies. \r\nSources: Literature; to: Variants in this gene can cause congenital anomalies, primarily affecting the brain. One report of CDH.\r\nSources: Literature","entity_name":"PDHA1","entity_type":"gene"},{"created":"2022-03-03T09:14:00.719128+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4632","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: PDHA1: Changed publications: 33461977, 26865159","entity_name":"PDHA1","entity_type":"gene"},{"created":"2022-03-03T09:12:40.655440+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4632","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Single individual reported as part of a cohort. Note variants in this gene can cause congenital anomalies. \nSources: Literature; to: Variants in this gene can cause congenital anomalies. \r\nSources: Literature","entity_name":"PDHA1","entity_type":"gene"},{"created":"2022-03-03T09:12:29.776265+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4632","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: PDHA1: Changed rating: GREEN; Changed phenotypes: Pyruvate dehydrogenase E1-alpha deficiency, MIM# 312170","entity_name":"PDHA1","entity_type":"gene"},{"created":"2022-03-03T09:11:23.194010+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4632","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX1 as ready","entity_name":"PEX1","entity_type":"gene"},{"created":"2022-03-03T09:11:23.185040+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4632","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex1 has been classified as Green List (High Evidence).","entity_name":"PEX1","entity_type":"gene"},{"created":"2022-03-03T09:11:19.425085+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4632","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX1 were changed from PEROXISOME BIOGENESIS DISORDER COMPLEMENTATION GROUP 1; INFANTILE REFSUM DISEASE; ADRENOLEUKODYSTROPHY NEONATAL to Peroxisome biogenesis disorder 1A (Zellweger) (MIM#214100)","entity_name":"PEX1","entity_type":"gene"},{"created":"2022-03-03T09:11:05.879848+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4631","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX1 were set to ","entity_name":"PEX1","entity_type":"gene"},{"created":"2022-03-03T09:10:33.724781+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4630","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX10 as ready","entity_name":"PEX10","entity_type":"gene"},{"created":"2022-03-03T09:10:33.713755+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4630","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex10 has been classified as Green List (High Evidence).","entity_name":"PEX10","entity_type":"gene"}]}