{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1170","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1168","results":[{"created":"2021-10-24T17:55:44.570595+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WRAP53 was added\ngene: WRAP53 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WRAP53 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: WRAP53 were set to DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 3","entity_name":"WRAP53","entity_type":"gene"},{"created":"2021-10-24T17:55:43.971013+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WNT7A was added\ngene: WNT7A was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WNT7A was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: WNT7A were set to FUHRMANN SYNDROME; LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME","entity_name":"WNT7A","entity_type":"gene"},{"created":"2021-10-24T17:55:43.657244+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WNT5A was added\ngene: WNT5A was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WNT5A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: WNT5A were set to WNT5A-RELATED ROBINOW SYNDROME, AUTOSOMAL DOMINANT","entity_name":"WNT5A","entity_type":"gene"},{"created":"2021-10-24T17:55:43.273632+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WNT10B was added\ngene: WNT10B was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WNT10B was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: WNT10B were set to Split-hand/foot malformation 6, OMIM:225300","entity_name":"WNT10B","entity_type":"gene"},{"created":"2021-10-24T17:55:42.751109+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WNT1 was added\ngene: WNT1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WNT1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: WNT1 were set to Osteogenesis imperfecta, type XV, OMIM:615220","entity_name":"WNT1","entity_type":"gene"},{"created":"2021-10-24T17:55:42.364171+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR62 was added\ngene: WDR62 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WDR62 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: WDR62 were set to MICROCEPHALY CORTICAL MALFORMATIONS AND MENTAL RETARDATION","entity_name":"WDR62","entity_type":"gene"},{"created":"2021-10-24T17:55:42.045241+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR60 was added\ngene: WDR60 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WDR60 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: WDR60 were set to SHORT-RIB POLYDACTYLY; JEUNE SYNDROMES","entity_name":"WDR60","entity_type":"gene"},{"created":"2021-10-24T17:55:41.456715+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR35 was added\ngene: WDR35 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WDR35 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: WDR35 were set to CRANIOECTODERMAL DYSPLASIA 2; SHORT RIB-POLYDACTYLY SYNDROME, TYPE V","entity_name":"WDR35","entity_type":"gene"},{"created":"2021-10-24T17:55:41.067365+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR34 was added\ngene: WDR34 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WDR34 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: WDR34 were set to SHORT-RIB POLYDACTYLY SYNDROME TYPE III; SEVERE ASPHYXIATING THORACIC DYSPLASIA","entity_name":"WDR34","entity_type":"gene"},{"created":"2021-10-24T17:55:40.751908+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR26 was added\ngene: WDR26 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WDR26 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: WDR26 were set to Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features","entity_name":"WDR26","entity_type":"gene"},{"created":"2021-10-24T17:55:40.162654+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDR19 was added\ngene: WDR19 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WDR19 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: WDR19 were set to CRANIOECTODERMAL DYSPLASIA 4; ASPHYXIATING THORACIC DYSTROPHY 5","entity_name":"WDR19","entity_type":"gene"},{"created":"2021-10-24T17:55:39.848207+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WDPCP was added\ngene: WDPCP was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: WDPCP was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: WDPCP were set to BARDET-BIEDL SYNDROME TYPE 15","entity_name":"WDPCP","entity_type":"gene"},{"created":"2021-10-24T17:55:39.462720+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VSX2 was added\ngene: VSX2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: VSX2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: VSX2 were set to MICROPHTHALMIA ISOLATED TYPE 2; MICROPHTHALMIA WITH CATARACTS AND IRIS ABNORMALITIES; MICROPHTHALMIA ISOLATED WITH COLOBOMA TYPE 3","entity_name":"VSX2","entity_type":"gene"},{"created":"2021-10-24T17:55:39.147608+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VPS53 was added\ngene: VPS53 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: VPS53 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: VPS53 were set to 12920088; 24577744; 30100179\nPhenotypes for gene: VPS53 were set to Progressive cerebella-cerebral atrophy type 2; PONTOCEREBELLAR HYPOPLASIA, TYPE 2E 615851","entity_name":"VPS53","entity_type":"gene"},{"created":"2021-10-24T17:55:38.558926+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VPS33B was added\ngene: VPS33B was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: VPS33B was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: VPS33B were set to ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1","entity_name":"VPS33B","entity_type":"gene"},{"created":"2021-10-24T17:55:38.174507+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VPS13B was added\ngene: VPS13B was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: VPS13B was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: VPS13B were set to 20683995\nPhenotypes for gene: VPS13B were set to COHEN SYNDROME","entity_name":"VPS13B","entity_type":"gene"},{"created":"2021-10-24T17:55:37.856830+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VLDLR was added\ngene: VLDLR was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: VLDLR was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: VLDLR were set to CEREBELLAR ATAXIA MENTAL RETARDATION AND DYSEQUILIBRIUM SYNDROME TYPE 1","entity_name":"VLDLR","entity_type":"gene"},{"created":"2021-10-24T17:55:37.266641+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: VIPAS39 was added\ngene: VIPAS39 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: VIPAS39 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: VIPAS39 were set to ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2021-10-24T17:55:36.951915+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UROS was added\ngene: UROS was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: UROS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: UROS were set to CONGENITAL ERYTHROPOIETIC PORPHYRIA","entity_name":"UROS","entity_type":"gene"},{"created":"2021-10-24T17:55:36.562614+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UMPS was added\ngene: UMPS was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: UMPS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: UMPS were set to OROTIC ACIDURIA TYPE 1","entity_name":"UMPS","entity_type":"gene"},{"created":"2021-10-24T17:55:36.049163+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UBR1 was added\ngene: UBR1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: UBR1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: UBR1 were set to JOHANSON-BLIZZARD SYNDROME","entity_name":"UBR1","entity_type":"gene"},{"created":"2021-10-24T17:55:35.661875+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UBE3B was added\ngene: UBE3B was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: UBE3B was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: UBE3B were set to BLEPHAROPHIMOSIS-MENTAL RETARDATION","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-10-24T17:55:35.347538+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UBA1 was added\ngene: UBA1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: UBA1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: UBA1 were set to Spinal muscular atrophy, X-linked 2, infantile 301830","entity_name":"UBA1","entity_type":"gene"},{"created":"2021-10-24T17:55:34.752613+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TXNL4A was added\ngene: TXNL4A was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TXNL4A was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TXNL4A were set to BURN MCKEOWN SYNDROME","entity_name":"TXNL4A","entity_type":"gene"},{"created":"2021-10-24T17:55:34.365345+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TWIST2 was added\ngene: TWIST2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TWIST2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: TWIST2 were set to 26119818\nPhenotypes for gene: TWIST2 were set to Ablepharon-macrostomia syndrome, 200110; Barber-Say syndrome, 209885\nMode of pathogenicity for gene: TWIST2 was set to Other","entity_name":"TWIST2","entity_type":"gene"},{"created":"2021-10-24T17:55:34.051700+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TWIST1 was added\ngene: TWIST1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TWIST1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TWIST1 were set to SAETHRE-CHOTZEN SYNDROME; CRANIOSYNOSTOSIS, TYPE 1","entity_name":"TWIST1","entity_type":"gene"},{"created":"2021-10-24T17:55:33.463664+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBGCP6 was added\ngene: TUBGCP6 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TUBGCP6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TUBGCP6 were set to MICROCEPHALY AND CHORIORETINOPATHY WITH OR WITHOUT MENTAL RETARDATION","entity_name":"TUBGCP6","entity_type":"gene"},{"created":"2021-10-24T17:55:33.149151+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBB4A was added\ngene: TUBB4A was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TUBB4A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TUBB4A were set to HYPOMYELINATION WITH ATROPHY OF THE BASAL GANGLIA AND CEREBELLUM","entity_name":"TUBB4A","entity_type":"gene"},{"created":"2021-10-24T17:55:32.671269+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBB2B was added\ngene: TUBB2B was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TUBB2B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TUBB2B were set to POLYMICROGYRIA ASYMMETRIC","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-10-24T17:55:32.155901+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBB2A was added\ngene: TUBB2A was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TUBB2A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: TUBB2A were set to 28840640; 30016746; 25326637; 27770045; 24702957\nPhenotypes for gene: TUBB2A were set to Cortical dysplasia, complex, with other brain malformations 5, OMIM:615763; Complex cortical dysplasia with other brain malformations 5, MONDO:0014337\nMode of pathogenicity for gene: TUBB2A was set to Other","entity_name":"TUBB2A","entity_type":"gene"},{"created":"2021-10-24T17:55:31.755672+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBB was added\ngene: TUBB was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TUBB was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TUBB were set to CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; Circumferential Skin Creases Kunze Type","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-10-24T17:55:31.369255+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBA8 was added\ngene: TUBA8 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TUBA8 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TUBA8 were set to 28388629; 31481326; 19896110\nPhenotypes for gene: TUBA8 were set to Cortical dysplasia, complex, with other brain malformations 8, 613180; POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA","entity_name":"TUBA8","entity_type":"gene"},{"created":"2021-10-24T17:55:31.055378+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TUBA1A was added\ngene: TUBA1A was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TUBA1A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TUBA1A were set to INTELLECTUAL DISABILITY; LISSENCEPHALY TYPE 3","entity_name":"TUBA1A","entity_type":"gene"},{"created":"2021-10-24T17:55:30.465339+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TTN was added\ngene: TTN was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TTN was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TTN were set to 29575618; 28040389; 29691892\nPhenotypes for gene: TTN were set to congenital titinopathy with arthrogryposis","entity_name":"TTN","entity_type":"gene"},{"created":"2021-10-24T17:55:30.151825+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TTC8 was added\ngene: TTC8 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TTC8 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TTC8 were set to RETINITIS PIGMENTOSA TYPE 51; BARDET-BIEDL SYNDROME TYPE 8","entity_name":"TTC8","entity_type":"gene"},{"created":"2021-10-24T17:55:29.763240+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TTC7A was added\ngene: TTC7A was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TTC7A was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TTC7A were set to INTESTINAL ATRESIA, MULTIPLE","entity_name":"TTC7A","entity_type":"gene"},{"created":"2021-10-24T17:55:29.246168+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TTC37 was added\ngene: TTC37 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TTC37 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TTC37 were set to TRICHOHEPATOENTERIC SYNDROME","entity_name":"TTC37","entity_type":"gene"},{"created":"2021-10-24T17:55:28.858915+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TTC21B was added\ngene: TTC21B was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TTC21B was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TTC21B were set to Short-rib thoracic dysplasia 4 with or without polydactyly 613819","entity_name":"TTC21B","entity_type":"gene"},{"created":"2021-10-24T17:55:28.547603+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TSEN54 was added\ngene: TSEN54 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TSEN54 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TSEN54 were set to 16470708; 20952379; 20956791\nPhenotypes for gene: TSEN54 were set to ?Pontocerebellar hypoplasia type 5, OMIM:610204; Pontocerebellar hypoplasia type 4, OMIM:225753; Pontocerebellar hypoplasia type 2A, OMIM:277470","entity_name":"TSEN54","entity_type":"gene"},{"created":"2021-10-24T17:55:27.959536+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TSC2 was added\ngene: TSC2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TSC2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TSC2 were set to TUBEROUS SCLEROSIS TYPE 2; LYMPHANGIOLEIOMYOMATOSIS","entity_name":"TSC2","entity_type":"gene"},{"created":"2021-10-24T17:55:27.578824+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TSC1 was added\ngene: TSC1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TSC1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TSC1 were set to TUBEROUS SCLEROSIS TYPE 1","entity_name":"TSC1","entity_type":"gene"},{"created":"2021-10-24T17:55:27.267071+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRPV6 was added\ngene: TRPV6 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TRPV6 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TRPV6 were set to 29861107\nPhenotypes for gene: TRPV6 were set to Hyperparathyroidism, transient neonatal, 618188; Transient Neonatal Hyperparathyroidism","entity_name":"TRPV6","entity_type":"gene"},{"created":"2021-10-24T17:55:26.666848+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRPV4 was added\ngene: TRPV4 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TRPV4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TRPV4 were set to METATROPIC DYSPLASIA; SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE","entity_name":"TRPV4","entity_type":"gene"},{"created":"2021-10-24T17:55:26.354568+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRPS1 was added\ngene: TRPS1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TRPS1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TRPS1 were set to TRICHO-RHINO-PHALANGEAL SYNDROME TYPE 1","entity_name":"TRPS1","entity_type":"gene"},{"created":"2021-10-24T17:55:25.963931+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRIP4 was added\ngene: TRIP4 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TRIP4 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TRIP4 were set to 26924529; 27008887\nPhenotypes for gene: TRIP4 were set to Prenatal-onset spinal muscular atrophy with congenital bone fractures, MONDO:0000209; Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome, MONDO:0014896; ?Muscular dystrophy, congenital, Davignon-Chauveau type, OMIM:617066; Spinal muscular atrophy with congenital bone fractures 1, OMIM:616866; Spinal muscular atrophy with congenital bone fractures 1, MONDO:0014806","entity_name":"TRIP4","entity_type":"gene"},{"created":"2021-10-24T17:55:25.654727+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRIP12 was added\ngene: TRIP12 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TRIP12 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TRIP12 were set to TRIP12-related intellectual disability with/without autism spectrum disorder","entity_name":"TRIP12","entity_type":"gene"},{"created":"2021-10-24T17:55:25.073522+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRIP11 was added\ngene: TRIP11 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TRIP11 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TRIP11 were set to ACHONDROGENESIS TYPE 1A","entity_name":"TRIP11","entity_type":"gene"},{"created":"2021-10-24T17:55:24.754764+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRIM37 was added\ngene: TRIM37 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TRIM37 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TRIM37 were set to MULIBREY NANISM","entity_name":"TRIM37","entity_type":"gene"},{"created":"2021-10-24T17:55:24.369995+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TREX1 was added\ngene: TREX1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TREX1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TREX1 were set to AICARDI-GOUTIERES SYNDROME 1, DOMINANT AND RECESSIVE","entity_name":"TREX1","entity_type":"gene"},{"created":"2021-10-24T17:55:23.853819+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRAPPC9 was added\ngene: TRAPPC9 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TRAPPC9 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TRAPPC9 were set to MENTAL RETARDATION AUTOSOMAL RECESSIVE TYPE 13","entity_name":"TRAPPC9","entity_type":"gene"},{"created":"2021-10-24T17:55:23.469472+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRAF7 was added\ngene: TRAF7 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TRAF7 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: TRAF7 were set to 29961569\nPhenotypes for gene: TRAF7 were set to Developmental Delay, Congenital Anomalies, and Dysmorphic Features; Cardiac, facial, and digital anomalies with developmental delay, 618164\nMode of pathogenicity for gene: TRAF7 was set to Other - please provide details in the comments","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-10-24T17:55:23.159996+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TPM3 was added\ngene: TPM3 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TPM3 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: TPM3 were set to Congenital fiber-type disproportion myopathy 255310","entity_name":"TPM3","entity_type":"gene"},{"created":"2021-10-24T17:55:22.572706+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TPM2 was added\ngene: TPM2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TPM2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: TPM2 were set to 12592607; 17339586\nPhenotypes for gene: TPM2 were set to Arthrogryposis multiplex congenita, distal, type 1, 108120; Arthrogryposis, distal, type 2B, 601680; ARTHROGRYPOSIS, DISTAL, TYPE 1\nMode of pathogenicity for gene: TPM2 was set to Other","entity_name":"TPM2","entity_type":"gene"},{"created":"2021-10-24T17:55:22.255431+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TP63 was added\ngene: TP63 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TP63 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TP63 were set to ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE; ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME; ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFT LIP/PALATE SYNDROME TYPE 3; SPLIT-HAND/FOOT MALFORMATION TYPE 4; ECTODERMAL DYSPLASIA RAPP-HODGKIN TYPE; NON-SYNDROMIC OROFACIAL CLEFT TYPE 8; LIMB-MAMMARY SYNDROME","entity_name":"TP63","entity_type":"gene"},{"created":"2021-10-24T17:55:21.867826+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TOP3A was added\ngene: TOP3A was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TOP3A was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TOP3A were set to 30193137\nPhenotypes for gene: TOP3A were set to Bloom Syndrome like Disorder","entity_name":"TOP3A","entity_type":"gene"},{"created":"2021-10-24T17:55:21.349451+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TNNT1 was added\ngene: TNNT1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TNNT1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TNNT1 were set to Nemaline myopathy, Amish type 605355","entity_name":"TNNT1","entity_type":"gene"},{"created":"2021-10-24T17:55:20.962064+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TNNI2 was added\ngene: TNNI2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TNNI2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TNNI2 were set to Arthrogryposis multiplex congenita, distal, type 2B 601680","entity_name":"TNNI2","entity_type":"gene"},{"created":"2021-10-24T17:55:20.651206+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM94 was added\ngene: TMEM94 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TMEM94 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TMEM94 were set to PMID: 30526868\nPhenotypes for gene: TMEM94 were set to Intellectual developmental disorder with cardiac defects and dysmorphic facies, OMIM:618316","entity_name":"TMEM94","entity_type":"gene"},{"created":"2021-10-24T17:55:20.266496+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM67 was added\ngene: TMEM67 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TMEM67 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TMEM67 were set to COACH SYNDROM; JOUBERT SYNDROME TYPE 6; MECKEL SYNDROME TYPE 3; NEPHRONOPHTHISIS TYPE 11","entity_name":"TMEM67","entity_type":"gene"},{"created":"2021-10-24T17:55:19.752458+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM5 was added\ngene: TMEM5 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TMEM5 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TMEM5 were set to SEVERE COBBLESTONE LISSENCEPHALY","entity_name":"TMEM5","entity_type":"gene"},{"created":"2021-10-24T17:55:19.367420+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM237 was added\ngene: TMEM237 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TMEM237 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TMEM237 were set to JOUBERT SYNDROME 14","entity_name":"TMEM237","entity_type":"gene"},{"created":"2021-10-24T17:55:19.053050+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM231 was added\ngene: TMEM231 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TMEM231 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TMEM231 were set to Joubert syndrome 20 614970; Meckel syndrome 11 615397","entity_name":"TMEM231","entity_type":"gene"},{"created":"2021-10-24T17:55:18.462305+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM165 was added\ngene: TMEM165 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TMEM165 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TMEM165 were set to CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK","entity_name":"TMEM165","entity_type":"gene"},{"created":"2021-10-24T17:55:18.152163+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMEM138 was added\ngene: TMEM138 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TMEM138 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TMEM138 were set to Joubert syndrome 16 614465","entity_name":"TMEM138","entity_type":"gene"},{"created":"2021-10-24T17:55:17.765918+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TMCO1 was added\ngene: TMCO1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TMCO1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TMCO1 were set to CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME","entity_name":"TMCO1","entity_type":"gene"},{"created":"2021-10-24T17:55:17.458295+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TINF2 was added\ngene: TINF2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TINF2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TINF2 were set to EXUDATIVE RETINOPATHY WITH BONE MARROW FAILURE","entity_name":"TINF2","entity_type":"gene"},{"created":"2021-10-24T17:55:16.866337+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: THRA was added\ngene: THRA was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: THRA was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: THRA were set to HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6","entity_name":"THRA","entity_type":"gene"},{"created":"2021-10-24T17:55:16.559509+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: THOC6 was added\ngene: THOC6 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: THOC6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: THOC6 were set to Beaulieu-Boycott-Innes syndrome","entity_name":"THOC6","entity_type":"gene"},{"created":"2021-10-24T17:55:16.248268+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TGM1 was added\ngene: TGM1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TGM1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TGM1 were set to Ichthyosis, congenital, autosomal recessive 242300","entity_name":"TGM1","entity_type":"gene"},{"created":"2021-10-24T17:55:15.661756+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TGIF1 was added\ngene: TGIF1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TGIF1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TGIF1 were set to HOLOPROSENCEPHALY; Holoprosencephaly 4 142946","entity_name":"TGIF1","entity_type":"gene"},{"created":"2021-10-24T17:55:15.354785+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TGFBR2 was added\ngene: TGFBR2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TGFBR2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TGFBR2 were set to LOEYS-DIETZ SYNDROME; TGFBR2-RELATED LOEYS-DIETZ SYNDROME","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2021-10-24T17:55:14.969449+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TGFBR1 was added\ngene: TGFBR1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TGFBR1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TGFBR1 were set to LOEYS-DIETZ SYNDROME TYPE 2A; AORTIC ANEURYSM FAMILIAL THORACIC TYPE 5; LOEYS-DIETZ SYNDROME TYPE 1A","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2021-10-24T17:55:14.457031+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TGFB3 was added\ngene: TGFB3 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TGFB3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TGFB3 were set to LOEYS-DIETZ SYNDROME","entity_name":"TGFB3","entity_type":"gene"},{"created":"2021-10-24T17:55:14.149322+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TGFB2 was added\ngene: TGFB2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TGFB2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TGFB2 were set to LOEYS-DIETZ SYNDROME, TYPE 4","entity_name":"TGFB2","entity_type":"gene"},{"created":"2021-10-24T17:55:13.764183+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TGDS was added\ngene: TGDS was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TGDS was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TGDS were set to CATEL-MANZKE SYNDROME","entity_name":"TGDS","entity_type":"gene"},{"created":"2021-10-24T17:55:13.457684+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TFAP2B was added\ngene: TFAP2B was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TFAP2B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TFAP2B were set to CHAR SYNDROME","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2021-10-24T17:55:12.867380+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TFAP2A was added\ngene: TFAP2A was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TFAP2A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TFAP2A were set to BRANCHIOOCULOFACIAL SYNDROME","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2021-10-24T17:55:12.559321+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TCTN3 was added\ngene: TCTN3 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TCTN3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TCTN3 were set to MOHR-MAJEWSKI SYNDROME","entity_name":"TCTN3","entity_type":"gene"},{"created":"2021-10-24T17:55:12.249919+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TCTN2 was added\ngene: TCTN2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TCTN2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TCTN2 were set to 30712880\nPhenotypes for gene: TCTN2 were set to JOUBERT SYNDROME AND RELATED DISORDERS","entity_name":"TCTN2","entity_type":"gene"},{"created":"2021-10-24T17:55:11.560260+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TCTN1 was added\ngene: TCTN1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TCTN1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TCTN1 were set to Joubert syndrome 13 614173; JOUBERT SYNDROME AND RELATED DISORDERS","entity_name":"TCTN1","entity_type":"gene"},{"created":"2021-10-24T17:55:11.253772+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TCOF1 was added\ngene: TCOF1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TCOF1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TCOF1 were set to TREACHER COLLINS SYNDROME TYPE 1","entity_name":"TCOF1","entity_type":"gene"},{"created":"2021-10-24T17:55:10.864528+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TCIRG1 was added\ngene: TCIRG1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TCIRG1 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TCIRG1 were set to Osteopetrosis, infantile malignant 259700","entity_name":"TCIRG1","entity_type":"gene"},{"created":"2021-10-24T17:55:10.553141+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TCF4 was added\ngene: TCF4 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TCF4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TCF4 were set to PITT-HOPKINS SYNDROME","entity_name":"TCF4","entity_type":"gene"},{"created":"2021-10-24T17:55:09.964970+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TCF12 was added\ngene: TCF12 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TCF12 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TCF12 were set to CORONAL CRANIOSYNOSTOSIS","entity_name":"TCF12","entity_type":"gene"},{"created":"2021-10-24T17:55:09.656998+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBX6 was added\ngene: TBX6 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBX6 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TBX6 were set to Spondylocostal dysostosis 5 122600","entity_name":"TBX6","entity_type":"gene"},{"created":"2021-10-24T17:55:09.347150+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBX5 was added\ngene: TBX5 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBX5 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TBX5 were set to HOLT-ORAM SYNDROME","entity_name":"TBX5","entity_type":"gene"},{"created":"2021-10-24T17:55:08.757718+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBX4 was added\ngene: TBX4 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBX4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TBX4 were set to Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension, OMIM:147891","entity_name":"TBX4","entity_type":"gene"},{"created":"2021-10-24T17:55:08.449982+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBX3 was added\ngene: TBX3 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBX3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TBX3 were set to ULNAR-MAMMARY SYNDROME","entity_name":"TBX3","entity_type":"gene"},{"created":"2021-10-24T17:55:08.066069+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBX20 was added\ngene: TBX20 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBX20 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TBX20 were set to ATRIAL SEPTAL DEFECT TYPE 4","entity_name":"TBX20","entity_type":"gene"},{"created":"2021-10-24T17:55:07.557538+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBX18 was added\ngene: TBX18 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBX18 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TBX18 were set to CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2","entity_name":"TBX18","entity_type":"gene"},{"created":"2021-10-24T17:55:07.248240+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBX15 was added\ngene: TBX15 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBX15 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TBX15 were set to Cousin Syndrome; Craniofacial Dysmorphism, Hypoplasia of Scapula and Pelvis, and Short Stature","entity_name":"TBX15","entity_type":"gene"},{"created":"2021-10-24T17:55:06.863763+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBX1 was added\ngene: TBX1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBX1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPhenotypes for gene: TBX1 were set to 22Q11.2 DELETION SYNDROME","entity_name":"TBX1","entity_type":"gene"},{"created":"2021-10-24T17:55:06.557820+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBL1XR1 was added\ngene: TBL1XR1 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBL1XR1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: TBL1XR1 were set to 26769062; 30365874; 25425123; 9450851; 23160955; 28687524; 23176139; 16007632\nPhenotypes for gene: TBL1XR1 were set to Intellectual disability with autism spectrum disorder; Pierpont syndrome","entity_name":"TBL1XR1","entity_type":"gene"},{"created":"2021-10-24T17:55:05.969634+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBCK was added\ngene: TBCK was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBCK was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TBCK were set to Severe Infantile Syndromic Encephalopathy","entity_name":"TBCK","entity_type":"gene"},{"created":"2021-10-24T17:55:05.663000+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBCE was added\ngene: TBCE was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBCE was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TBCE were set to HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; Early-Onset Progressive Encephalopathy with Distal Spinal Muscular Atrophy; KENNY-CAFFEY SYNDROME TYPE 1","entity_name":"TBCE","entity_type":"gene"},{"created":"2021-10-24T17:55:05.357285+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBCD was added\ngene: TBCD was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBCD was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TBCD were set to Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome, MONDO:0044646; Encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum, OMIM:617193","entity_name":"TBCD","entity_type":"gene"},{"created":"2021-10-24T17:55:04.773012+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBC1D24 was added\ngene: TBC1D24 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBC1D24 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TBC1D24 were set to NON SYNDROMAL HEARING LOSS; DOORS SYNDROME; MYOCLONIC EPILEPSY, INFANTILE, FAMILIAL","entity_name":"TBC1D24","entity_type":"gene"},{"created":"2021-10-24T17:55:04.461898+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBC1D23 was added\ngene: TBC1D23 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBC1D23 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TBC1D23 were set to Non-degenerative Pontocerebellar Hypoplasia","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2021-10-24T17:55:04.150612+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TBC1D20 was added\ngene: TBC1D20 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBC1D20 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TBC1D20 were set to 24239381\nPhenotypes for gene: TBC1D20 were set to Warburg micro syndrome 4; Warburg micro syndrome 4 615663","entity_name":"TBC1D20","entity_type":"gene"},{"created":"2021-10-24T17:55:03.772255+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TAZ was added\ngene: TAZ was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TAZ was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: TAZ were set to BARTH SYNDROME","entity_name":"TAZ","entity_type":"gene"}]}