{"count":220790,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=990","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=988","results":[{"created":"2022-02-17T09:36:20.046892+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3580","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RORA as ready","entity_name":"RORA","entity_type":"gene"},{"created":"2022-02-17T09:36:20.035619+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3580","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rora has been classified as Amber List (Moderate Evidence).","entity_name":"RORA","entity_type":"gene"},{"created":"2022-02-17T09:36:16.359615+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3580","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RORA were changed from INTELLECTUAL DISABILITY to Intellectual developmental disorder with or without epilepsy or cerebellar ataxia, MIM#618060","entity_name":"RORA","entity_type":"gene"},{"created":"2022-02-17T09:35:56.146239+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3579","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RORA were set to ","entity_name":"RORA","entity_type":"gene"},{"created":"2022-02-17T09:35:44.443758+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3578","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: RORA was changed from Other to None","entity_name":"RORA","entity_type":"gene"},{"created":"2022-02-17T09:35:29.826865+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3577","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: RORA was changed from  to Other","entity_name":"RORA","entity_type":"gene"},{"created":"2022-02-17T09:35:20.512678+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3576","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RORA was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RORA","entity_type":"gene"},{"created":"2022-02-17T09:35:07.898574+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3575","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Eleven unrelated individuals with de novo variants in this gene; postulated that some variants exert dominant-negative effect resulting in a more severe phenotype than the LoF variants. \nSources: Expert list; to: Eleven unrelated individuals with de novo variants in this gene; postulated that some variants exert dominant-negative effect resulting in a more severe phenotype than the LoF variants.\r\n\r\nClinical presentation is generally post-natal, but pontocerebellar hypoplasia rarely reported.\r\n\r\nSources: Expert list","entity_name":"RORA","entity_type":"gene"},{"created":"2022-02-17T09:34:40.590897+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3575","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RORA: Changed rating: AMBER","entity_name":"RORA","entity_type":"gene"},{"created":"2022-02-17T09:21:21.169351+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3575","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ROBO3 as ready","entity_name":"ROBO3","entity_type":"gene"},{"created":"2022-02-17T09:21:21.155673+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3575","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: robo3 has been classified as Green List (High Evidence).","entity_name":"ROBO3","entity_type":"gene"},{"created":"2022-02-17T09:21:16.962177+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3575","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ROBO3 were set to ","entity_name":"ROBO3","entity_type":"gene"},{"created":"2022-02-17T09:20:50.339006+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3574","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ROBO3 as Green List (high evidence)","entity_name":"ROBO3","entity_type":"gene"},{"created":"2022-02-17T09:20:50.325336+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3574","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: robo3 has been classified as Green List (High Evidence).","entity_name":"ROBO3","entity_type":"gene"},{"created":"2022-02-17T09:19:22.015187+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3573","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RMND1 as ready","entity_name":"RMND1","entity_type":"gene"},{"created":"2022-02-17T09:19:22.002724+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3573","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rmnd1 has been classified as Green List (High Evidence).","entity_name":"RMND1","entity_type":"gene"},{"created":"2022-02-17T09:19:00.499094+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3573","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RMND1 were changed from ENCEPHALOPATHY ASSOCIATED WITH MULTIPLE OXIDATIVE PHOSPHORYLATION COMPLEX DEFICIENCIES AND A MITOCHONDRIAL TRANSLATION DEFECT to Combined oxidative phosphorylation deficiency 11, MIM# MIM#614922","entity_name":"RMND1","entity_type":"gene"},{"created":"2022-02-17T09:18:45.748682+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3572","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RMND1 were set to ","entity_name":"RMND1","entity_type":"gene"},{"created":"2022-02-17T09:18:32.386004+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3571","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RMND1 as Green List (high evidence)","entity_name":"RMND1","entity_type":"gene"},{"created":"2022-02-17T09:18:32.373150+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3571","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rmnd1 has been classified as Green List (High Evidence).","entity_name":"RMND1","entity_type":"gene"},{"created":"2022-02-17T09:18:19.359087+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3570","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RMND1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Combined oxidative phosphorylation deficiency 11, MIM# MIM#614922; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RMND1","entity_type":"gene"},{"created":"2022-02-17T09:16:40.156276+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3570","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RLIM as ready","entity_name":"RLIM","entity_type":"gene"},{"created":"2022-02-17T09:16:40.143198+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3570","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rlim has been classified as Green List (High Evidence).","entity_name":"RLIM","entity_type":"gene"},{"created":"2022-02-17T09:16:36.768168+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3570","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RLIM were changed from INTELLECTUAL DISABILITY to Tonne-Kalscheuer syndrome, MIM# 300978","entity_name":"RLIM","entity_type":"gene"},{"created":"2022-02-17T09:16:23.254185+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3569","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RLIM were set to ","entity_name":"RLIM","entity_type":"gene"},{"created":"2022-02-17T09:16:09.201438+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3568","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RLIM as Green List (high evidence)","entity_name":"RLIM","entity_type":"gene"},{"created":"2022-02-17T09:16:09.190775+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3568","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rlim has been classified as Green List (High Evidence).","entity_name":"RLIM","entity_type":"gene"},{"created":"2022-02-17T09:15:00.307843+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3567","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RIN2 as ready","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-17T09:15:00.292554+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3567","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rin2 has been classified as Green List (High Evidence).","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-17T09:14:56.529528+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3567","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RIN2 were changed from MACROCEPHALY, ALOPECIA, CUTIS LAXA, AND SCOLIOSIS TALL FOREHEAD, SPARSE HAIR, SKIN HYPEREXTENSIBILITY, AND SCOLIOSIS to Macrocephaly, alopecia, cutis laxa, and scoliosis, MIM#613075","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-17T09:14:42.167985+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3566","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RIN2 were set to ","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-17T09:14:28.447727+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3565","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RIN2 as Green List (high evidence)","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-17T09:14:28.434591+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3565","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rin2 has been classified as Green List (High Evidence).","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-16T17:28:09.962454+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10999","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RIN2 as ready","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-16T17:28:09.952912+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10999","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rin2 has been classified as Green List (High Evidence).","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-16T17:27:40.293499+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10999","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RIN2 were changed from  to Macrocephaly, alopecia, cutis laxa, and scoliosis, MIM#613075","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-16T17:26:24.308750+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10998","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RIN2 were set to ","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-16T17:26:00.764073+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10997","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RIN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-16T16:55:19.417241+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10996","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RIN2: Rating: GREEN; Mode of pathogenicity: None; Publications: 19631308, 20424861, 20954239, 24449201, 30769224; Phenotypes: Macrocephaly, alopecia, cutis laxa, and scoliosis, MIM#613075; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-16T16:54:32.843756+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3564","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Macrocephaly, subcortical cysts and other brain abnormalities are a feature.; to: Macrocephaly, subcortical cysts and other brain abnormalities are a feature. More than 5 unrelated families reported.","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-16T16:54:19.755640+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3564","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RIN2: Changed publications: 19631308, 20424861, 20954239, 24449201, 30769224","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-16T16:52:49.444966+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3564","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: ID is not a key feature of this syndrome, most individuals described as having normal/borderline intellect.; to: Macrocephaly, subcortical cysts and other brain abnormalities are a feature.","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-16T16:52:26.854775+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3564","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RIN2: Changed rating: GREEN","entity_name":"RIN2","entity_type":"gene"},{"created":"2022-02-16T16:50:03.316386+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3564","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RFT1 as ready","entity_name":"RFT1","entity_type":"gene"},{"created":"2022-02-16T16:50:03.304360+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3564","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rft1 has been classified as Amber List (Moderate Evidence).","entity_name":"RFT1","entity_type":"gene"},{"created":"2022-02-16T16:49:56.395375+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3564","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RFT1 were set to ","entity_name":"RFT1","entity_type":"gene"},{"created":"2022-02-16T16:49:40.186118+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3563","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Bi-allelic variants are associated with DD/ID, seizures, deafness. More than 10 unrelated families reported.; to: Bi-allelic variants are associated with DD/ID, seizures, deafness. More than 10 unrelated families reported.\r\n\r\nClinical presentation is typically post-natal, though age of onset of microcephaly is uncertain.","entity_name":"RFT1","entity_type":"gene"},{"created":"2022-02-16T16:49:16.211164+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3563","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RFT1: Changed rating: AMBER","entity_name":"RFT1","entity_type":"gene"},{"created":"2022-02-16T16:47:28.228223+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3563","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RBM10 as ready","entity_name":"RBM10","entity_type":"gene"},{"created":"2022-02-16T16:47:28.212616+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3563","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rbm10 has been classified as Green List (High Evidence).","entity_name":"RBM10","entity_type":"gene"},{"created":"2022-02-16T16:45:37.279709+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3563","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RBM10 were set to ","entity_name":"RBM10","entity_type":"gene"},{"created":"2022-02-16T16:45:14.890738+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3562","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RBM10 as Green List (high evidence)","entity_name":"RBM10","entity_type":"gene"},{"created":"2022-02-16T16:45:14.881464+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3562","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rbm10 has been classified as Green List (High Evidence).","entity_name":"RBM10","entity_type":"gene"},{"created":"2022-02-16T16:44:51.726456+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3561","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"RBM10","entity_type":"gene"},{"created":"2022-02-16T16:44:46.602415+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3561","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RBM10: Added comment: Well established gene-disease association, multiple congenital anomalies.; Changed rating: GREEN; Changed publications: 20451169, 24259342, 30450804, 30189253","entity_name":"RBM10","entity_type":"gene"},{"created":"2022-02-16T16:30:39.657593+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3561","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: DUSP6: Rating: RED; Mode of pathogenicity: None; Publications: 23643382, 32389901; Phenotypes: Hypogonadotropic hypogonadism 19 with or without anosmia MIM615269; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DUSP6","entity_type":"gene"},{"created":"2022-02-16T16:29:00.470206+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3561","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RBBP8 as ready","entity_name":"RBBP8","entity_type":"gene"},{"created":"2022-02-16T16:29:00.457840+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3561","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rbbp8 has been classified as Green List (High Evidence).","entity_name":"RBBP8","entity_type":"gene"},{"created":"2022-02-16T16:28:55.988068+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3561","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RBBP8 were changed from Seckel syndrome 2, MONDO:0011715; Seckel syndrome 2, OMIM:606744 to Jawad syndrome, MIM# 251255; Seckel syndrome 2, MONDO:0011715; Seckel syndrome 2, OMIM:606744","entity_name":"RBBP8","entity_type":"gene"},{"created":"2022-02-16T16:28:42.606998+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3560","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RBBP8 were set to ","entity_name":"RBBP8","entity_type":"gene"},{"created":"2022-02-16T16:28:30.243180+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3559","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RBBP8 as Green List (high evidence)","entity_name":"RBBP8","entity_type":"gene"},{"created":"2022-02-16T16:28:30.230691+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3559","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rbbp8 has been classified as Green List (High Evidence).","entity_name":"RBBP8","entity_type":"gene"},{"created":"2022-02-16T16:27:47.717803+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3558","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAD51C as ready","entity_name":"RAD51C","entity_type":"gene"},{"created":"2022-02-16T16:27:47.707321+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3558","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rad51c has been classified as Green List (High Evidence).","entity_name":"RAD51C","entity_type":"gene"},{"created":"2022-02-16T16:27:43.781228+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3558","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAD51C were changed from FANCONI ANEMIA, COMPLEMENTATION GROUP 0 to Fanconi anemia, complementation group O, MIM# 613390","entity_name":"RAD51C","entity_type":"gene"},{"created":"2022-02-16T16:27:29.852349+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3557","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAD51C were set to ","entity_name":"RAD51C","entity_type":"gene"},{"created":"2022-02-16T16:27:16.402443+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3556","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RAD51C as Green List (high evidence)","entity_name":"RAD51C","entity_type":"gene"},{"created":"2022-02-16T16:27:16.393268+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3556","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rad51c has been classified as Green List (High Evidence).","entity_name":"RAD51C","entity_type":"gene"},{"created":"2022-02-16T16:26:37.678003+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3555","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAD51 as ready","entity_name":"RAD51","entity_type":"gene"},{"created":"2022-02-16T16:26:37.668125+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3555","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rad51 has been classified as Green List (High Evidence).","entity_name":"RAD51","entity_type":"gene"},{"created":"2022-02-16T16:26:33.759068+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3555","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAD51 were changed from MIRROR MOVEMENTS 2 to Fanconi anaemia, complementation group R, MIM# 617244","entity_name":"RAD51","entity_type":"gene"},{"created":"2022-02-16T16:25:19.181948+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3554","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAD51 were set to ","entity_name":"RAD51","entity_type":"gene"},{"created":"2022-02-16T16:25:03.983200+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3553","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAD51 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RAD51","entity_type":"gene"},{"created":"2022-02-16T16:24:52.807661+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3552","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RAD51 as Green List (high evidence)","entity_name":"RAD51","entity_type":"gene"},{"created":"2022-02-16T16:24:52.798315+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3552","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rad51 has been classified as Green List (High Evidence).","entity_name":"RAD51","entity_type":"gene"},{"created":"2022-02-16T16:24:41.179687+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3551","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Three unrelated individuals reported with de novo variants in this gene and FA phenotype. However, only one had radial ray abnormalities.\r\nSources: Expert Review; to: Three unrelated individuals reported with de novo variants in this gene and FA phenotype. \r\nSources: Expert Review","entity_name":"RAD51","entity_type":"gene"},{"created":"2022-02-16T16:24:31.492165+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3551","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RAD51: Changed rating: GREEN","entity_name":"RAD51","entity_type":"gene"},{"created":"2022-02-16T16:23:28.356317+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3551","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB11B as ready","entity_name":"RAB11B","entity_type":"gene"},{"created":"2022-02-16T16:23:28.345873+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3551","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab11b has been classified as Green List (High Evidence).","entity_name":"RAB11B","entity_type":"gene"},{"created":"2022-02-16T16:23:19.596979+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3551","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB11B were changed from INTELLECTUAL DISABILITY to Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter, MIM# 617807","entity_name":"RAB11B","entity_type":"gene"},{"created":"2022-02-16T16:22:53.710846+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3550","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB11B were set to ","entity_name":"RAB11B","entity_type":"gene"},{"created":"2022-02-16T16:22:41.705183+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3549","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAB11B was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RAB11B","entity_type":"gene"},{"created":"2022-02-16T16:22:31.800164+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3548","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RAB11B as Green List (high evidence)","entity_name":"RAB11B","entity_type":"gene"},{"created":"2022-02-16T16:22:31.790461+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3548","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab11b has been classified as Green List (High Evidence).","entity_name":"RAB11B","entity_type":"gene"},{"created":"2022-02-16T16:19:10.048248+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3547","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB11A as ready","entity_name":"RAB11A","entity_type":"gene"},{"created":"2022-02-16T16:19:10.029039+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3547","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab11a has been classified as Red List (Low Evidence).","entity_name":"RAB11A","entity_type":"gene"},{"created":"2022-02-16T16:19:05.534609+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3547","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB11A were set to ","entity_name":"RAB11A","entity_type":"gene"},{"created":"2022-02-16T16:18:53.739680+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3546","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAB11A was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RAB11A","entity_type":"gene"},{"created":"2022-02-16T16:18:43.755186+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3545","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RAB11A as Red List (low evidence)","entity_name":"RAB11A","entity_type":"gene"},{"created":"2022-02-16T16:18:43.745666+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3545","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab11a has been classified as Red List (Low Evidence).","entity_name":"RAB11A","entity_type":"gene"},{"created":"2022-02-16T16:18:32.237127+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3544","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Five individuals reported with DNMs and neurodevelopmental phenotypes as part of this paper; however, clinical details are sparse. Emerging gene, phenotype not yet clearly delineated. \nSources: Literature; to: Five individuals reported with DNMs and neurodevelopmental phenotypes as part of this paper; however, clinical details are sparse. Emerging gene, phenotype not yet clearly delineated.\r\n\r\nClinical presentation is post-natal.\r\nSources: Literature","entity_name":"RAB11A","entity_type":"gene"},{"created":"2022-02-16T16:17:47.759513+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3544","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RAB11A: Changed rating: RED","entity_name":"RAB11A","entity_type":"gene"},{"created":"2022-02-16T14:35:56.684940+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3544","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: DMP1: Rating: RED; Mode of pathogenicity: None; Publications: 17033625, 17033621, 31843680; Phenotypes: Hypophosphatemic rickets, AR MIM#241520; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"DMP1","entity_type":"gene"},{"created":"2022-02-16T14:23:04.757277+11:00","panel_name":"Renal Hypertension and Disorders of Aldosterone Metabolism","panel_id":190,"panel_version":"1.5","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: CYP11B1 as Green List (high evidence)","entity_name":"CYP11B1","entity_type":"gene"},{"created":"2022-02-16T14:23:04.747848+11:00","panel_name":"Renal Hypertension and Disorders of Aldosterone Metabolism","panel_id":190,"panel_version":"1.5","user_name":"Chirag Patel","item_type":"entity","text":"Gene: cyp11b1 has been classified as Green List (High Evidence).","entity_name":"CYP11B1","entity_type":"gene"},{"created":"2022-02-16T14:22:29.490775+11:00","panel_name":"Renal Hypertension and Disorders of Aldosterone Metabolism","panel_id":190,"panel_version":"1.4","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: CYP11B1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"CYP11B1","entity_type":"gene"},{"created":"2022-02-16T14:17:57.956546+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10996","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DLD as ready","entity_name":"DLD","entity_type":"gene"},{"created":"2022-02-16T14:17:57.945801+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10996","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dld has been classified as Green List (High Evidence).","entity_name":"DLD","entity_type":"gene"},{"created":"2022-02-16T14:17:50.137451+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10996","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DLD were changed from  to Dihydrolipoamide dehydrogenase deficiency MIM#246900","entity_name":"DLD","entity_type":"gene"},{"created":"2022-02-16T14:17:29.174444+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10995","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DLD were set to ","entity_name":"DLD","entity_type":"gene"}]}