{"count":220489,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=972","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=970","results":[{"created":"2022-02-23T16:43:29.781291+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4036","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRIP12 as ready","entity_name":"TRIP12","entity_type":"gene"},{"created":"2022-02-23T16:43:29.771743+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4036","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trip12 has been classified as Red List (Low Evidence).","entity_name":"TRIP12","entity_type":"gene"},{"created":"2022-02-23T16:43:25.414709+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4036","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRIP12 were changed from TRIP12-related intellectual disability with/without autism spectrum disorder to Mental retardation autosomal dominant 49, Clark-Baraitser Syndrome, MIM#617752","entity_name":"TRIP12","entity_type":"gene"},{"created":"2022-02-23T16:43:12.054302+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4035","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRIP12 were set to ","entity_name":"TRIP12","entity_type":"gene"},{"created":"2022-02-23T16:42:56.873173+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4034","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRIP12 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRIP12","entity_type":"gene"},{"created":"2022-02-23T16:42:47.424164+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4033","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRIP12 as Red List (low evidence)","entity_name":"TRIP12","entity_type":"gene"},{"created":"2022-02-23T16:42:47.410087+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4033","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trip12 has been classified as Red List (Low Evidence).","entity_name":"TRIP12","entity_type":"gene"},{"created":"2022-02-23T16:42:34.200852+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4032","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRIP12: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation autosomal dominant 49, Clark-Baraitser Syndrome, MIM#617752; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRIP12","entity_type":"gene"},{"created":"2022-02-23T16:41:19.936649+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4032","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRIP4 as ready","entity_name":"TRIP4","entity_type":"gene"},{"created":"2022-02-23T16:41:19.927938+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4032","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trip4 has been classified as Green List (High Evidence).","entity_name":"TRIP4","entity_type":"gene"},{"created":"2022-02-23T16:41:15.336330+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4032","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRIP4 were changed from 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 to 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":"2022-02-23T16:39:16.946875+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4031","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSEN54 as ready","entity_name":"TSEN54","entity_type":"gene"},{"created":"2022-02-23T16:39:16.935944+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4031","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tsen54 has been classified as Green List (High Evidence).","entity_name":"TSEN54","entity_type":"gene"},{"created":"2022-02-23T16:39:12.495435+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4031","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSEN54 were changed from ?Pontocerebellar hypoplasia type 5, OMIM:610204; Pontocerebellar hypoplasia type 4, OMIM:225753; Pontocerebellar hypoplasia type 2A, OMIM:277470 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":"2022-02-23T16:38:55.866440+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4030","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TSEN54 were set to 16470708; 20952379; 20956791","entity_name":"TSEN54","entity_type":"gene"},{"created":"2022-02-23T16:37:27.237371+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4029","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC21B as ready","entity_name":"TTC21B","entity_type":"gene"},{"created":"2022-02-23T16:37:27.226237+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4029","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc21b has been classified as Green List (High Evidence).","entity_name":"TTC21B","entity_type":"gene"},{"created":"2022-02-23T16:37:23.169243+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4029","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC21B were changed from Short-rib thoracic dysplasia 4 with or without polydactyly 613819 to Nephronophthisis 12, MIM# 613820; Short-rib thoracic dysplasia 4 with or without polydactyly, MIM# 613819","entity_name":"TTC21B","entity_type":"gene"},{"created":"2022-02-23T16:36:18.813953+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4028","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC21B were set to ","entity_name":"TTC21B","entity_type":"gene"},{"created":"2022-02-23T16:35:37.511792+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4027","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC8 as ready","entity_name":"TTC8","entity_type":"gene"},{"created":"2022-02-23T16:35:37.499791+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4027","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc8 has been classified as Green List (High Evidence).","entity_name":"TTC8","entity_type":"gene"},{"created":"2022-02-23T16:35:33.339719+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4027","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC8 were changed from RETINITIS PIGMENTOSA TYPE 51; BARDET-BIEDL SYNDROME TYPE 8 to Bardet-Biedl syndrome 8, MIM# 615985","entity_name":"TTC8","entity_type":"gene"},{"created":"2022-02-23T16:35:17.701689+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4026","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC8 were set to ","entity_name":"TTC8","entity_type":"gene"},{"created":"2022-02-23T16:34:43.813335+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4025","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTN as ready","entity_name":"TTN","entity_type":"gene"},{"created":"2022-02-23T16:34:43.798111+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4025","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttn has been classified as Green List (High Evidence).","entity_name":"TTN","entity_type":"gene"},{"created":"2022-02-23T16:34:38.873820+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4025","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTN were changed from congenital titinopathy with arthrogryposis to Salih myopathy; Muscular dystrophy, limb-girdle, autosomal recessive 10","entity_name":"TTN","entity_type":"gene"},{"created":"2022-02-23T16:34:24.130942+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4024","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTN were set to 29575618; 28040389; 29691892","entity_name":"TTN","entity_type":"gene"},{"created":"2022-02-23T16:33:35.246729+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4023","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB as ready","entity_name":"TUBB","entity_type":"gene"},{"created":"2022-02-23T16:33:35.236962+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4023","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb has been classified as Green List (High Evidence).","entity_name":"TUBB","entity_type":"gene"},{"created":"2022-02-23T16:33:30.473414+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4023","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBB were changed from CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; Circumferential Skin Creases Kunze Type to Cortical dysplasia, complex, with other brain malformations 6, MIM#615771","entity_name":"TUBB","entity_type":"gene"},{"created":"2022-02-23T16:33:16.752654+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4022","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB were set to ","entity_name":"TUBB","entity_type":"gene"},{"created":"2022-02-23T16:33:04.410463+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4021","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBB was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB","entity_type":"gene"},{"created":"2022-02-23T16:32:22.289744+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4020","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB2A as ready","entity_name":"TUBB2A","entity_type":"gene"},{"created":"2022-02-23T16:32:22.276360+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4020","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb2a has been classified as Green List (High Evidence).","entity_name":"TUBB2A","entity_type":"gene"},{"created":"2022-02-23T16:32:17.597950+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4020","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB2A were set to 28840640; 30016746; 25326637; 27770045; 24702957","entity_name":"TUBB2A","entity_type":"gene"},{"created":"2022-02-23T16:32:02.813371+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4019","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBB2A was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB2A","entity_type":"gene"},{"created":"2022-02-23T16:31:25.648305+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4018","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB2B as ready","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2022-02-23T16:31:25.634125+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4018","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb2b has been classified as Green List (High Evidence).","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2022-02-23T16:31:20.811821+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4018","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBB2B were changed from POLYMICROGYRIA ASYMMETRIC to Cortical dysplasia, complex, with other brain malformations 7 MIM#610031","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2022-02-23T16:31:07.329661+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4017","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB2B were set to ","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2022-02-23T16:30:21.331891+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4016","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBGCP6 as ready","entity_name":"TUBGCP6","entity_type":"gene"},{"created":"2022-02-23T16:30:21.321003+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4016","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubgcp6 has been classified as Green List (High Evidence).","entity_name":"TUBGCP6","entity_type":"gene"},{"created":"2022-02-23T16:30:17.379471+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4016","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBGCP6 were changed from MICROCEPHALY AND CHORIORETINOPATHY WITH OR WITHOUT MENTAL RETARDATION to Microcephaly and chorioretinopathy, autosomal recessive, 1, MIM#251270","entity_name":"TUBGCP6","entity_type":"gene"},{"created":"2022-02-23T16:30:02.698317+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4015","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBGCP6 were set to ","entity_name":"TUBGCP6","entity_type":"gene"},{"created":"2022-02-23T16:29:14.153419+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4014","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBA1 as ready","entity_name":"UBA1","entity_type":"gene"},{"created":"2022-02-23T16:29:14.143347+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4014","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uba1 has been classified as Green List (High Evidence).","entity_name":"UBA1","entity_type":"gene"},{"created":"2022-02-23T16:29:09.599765+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4014","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBA1 were changed from Spinal muscular atrophy, X-linked 2, infantile 301830 to Spinal muscular atrophy, X-linked 2, infantile, MIM# 301830","entity_name":"UBA1","entity_type":"gene"},{"created":"2022-02-23T16:28:56.079389+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4013","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBA1 were set to ","entity_name":"UBA1","entity_type":"gene"},{"created":"2022-02-23T16:28:00.663992+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4012","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBE3B as ready","entity_name":"UBE3B","entity_type":"gene"},{"created":"2022-02-23T16:28:00.624474+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4012","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ube3b has been classified as Green List (High Evidence).","entity_name":"UBE3B","entity_type":"gene"},{"created":"2022-02-23T16:27:53.901009+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4012","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBE3B were changed from BLEPHAROPHIMOSIS-MENTAL RETARDATION to Kaufman oculocerebrofacial syndrome, MIM# 244450; MONDO:0009485","entity_name":"UBE3B","entity_type":"gene"},{"created":"2022-02-23T16:27:35.702033+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4011","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBE3B were set to ","entity_name":"UBE3B","entity_type":"gene"},{"created":"2022-02-23T16:27:18.112958+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4010","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Intellectual disability, microcephaly, dysmorphic features, including blepharophimosis and ptosis. Over 20 families reported.; to: Intellectual disability, microcephaly, dysmorphic features, including blepharophimosis and ptosis. Congenital heart disease. Over 20 families reported.","entity_name":"UBE3B","entity_type":"gene"},{"created":"2022-02-23T16:26:23.209880+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4010","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBR1 as ready","entity_name":"UBR1","entity_type":"gene"},{"created":"2022-02-23T16:26:23.199146+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4010","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ubr1 has been classified as Green List (High Evidence).","entity_name":"UBR1","entity_type":"gene"},{"created":"2022-02-23T16:26:19.076641+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4010","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBR1 were changed from JOHANSON-BLIZZARD SYNDROME to Johanson-Blizzard syndrome (MIM#243800)","entity_name":"UBR1","entity_type":"gene"},{"created":"2022-02-23T16:26:06.268477+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4009","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBR1 were set to ","entity_name":"UBR1","entity_type":"gene"},{"created":"2022-02-23T16:25:26.637883+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4008","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UMPS as ready","entity_name":"UMPS","entity_type":"gene"},{"created":"2022-02-23T16:25:26.614103+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4008","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: umps has been classified as Green List (High Evidence).","entity_name":"UMPS","entity_type":"gene"},{"created":"2022-02-23T16:25:12.046921+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4008","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UMPS were changed from OROTIC ACIDURIA TYPE 1 to Orotic aciduria MIM# 258900","entity_name":"UMPS","entity_type":"gene"},{"created":"2022-02-23T16:24:57.513682+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4007","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UMPS were set to ","entity_name":"UMPS","entity_type":"gene"},{"created":"2022-02-23T16:24:08.145011+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4006","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VIPAS39 as ready","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-02-23T16:24:08.134619+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4006","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vipas39 has been classified as Green List (High Evidence).","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-02-23T16:24:04.284235+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4006","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VIPAS39 were changed from ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 to Arthrogryposis, renal dysfunction, and cholestasis 2, OMIM #613404","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-02-23T16:23:46.869441+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4005","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VIPAS39 were set to ","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-02-23T16:23:30.468656+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4004","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VIPAS39: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Arthrogryposis, renal dysfunction, and cholestasis 2, OMIM #613404; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-02-23T16:22:40.253615+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4004","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VPS13B as ready","entity_name":"VPS13B","entity_type":"gene"},{"created":"2022-02-23T16:22:40.243669+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4004","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps13b has been classified as Amber List (Moderate Evidence).","entity_name":"VPS13B","entity_type":"gene"},{"created":"2022-02-23T16:22:36.050026+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4004","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VPS13B were changed from COHEN SYNDROME to Cohen syndrome (MIM# 216550)","entity_name":"VPS13B","entity_type":"gene"},{"created":"2022-02-23T16:22:19.767424+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4003","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VPS13B as Amber List (moderate evidence)","entity_name":"VPS13B","entity_type":"gene"},{"created":"2022-02-23T16:22:19.756067+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4003","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps13b has been classified as Amber List (Moderate Evidence).","entity_name":"VPS13B","entity_type":"gene"},{"created":"2022-02-23T16:22:06.599635+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4002","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VPS13B: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Cohen syndrome (MIM# 216550); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VPS13B","entity_type":"gene"},{"created":"2022-02-23T16:20:25.694258+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4002","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VPS33B as ready","entity_name":"VPS33B","entity_type":"gene"},{"created":"2022-02-23T16:20:25.683030+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4002","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps33b has been classified as Green List (High Evidence).","entity_name":"VPS33B","entity_type":"gene"},{"created":"2022-02-23T16:20:20.132445+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4002","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VPS33B were changed from ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 to Arthrogryposis, renal dysfunction, and cholestasis 1 (MIM#208085)","entity_name":"VPS33B","entity_type":"gene"},{"created":"2022-02-23T16:20:06.499803+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4001","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VPS33B were set to ","entity_name":"VPS33B","entity_type":"gene"},{"created":"2022-02-23T16:19:28.926264+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4000","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VSX2 as ready","entity_name":"VSX2","entity_type":"gene"},{"created":"2022-02-23T16:19:28.914725+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4000","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vsx2 has been classified as Green List (High Evidence).","entity_name":"VSX2","entity_type":"gene"},{"created":"2022-02-23T16:18:21.480095+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4000","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VSX2 were changed from MICROPHTHALMIA ISOLATED TYPE 2; MICROPHTHALMIA WITH CATARACTS AND IRIS ABNORMALITIES; MICROPHTHALMIA ISOLATED WITH COLOBOMA TYPE 3 to Microphthalmia with coloboma 3, MIM# 610092; Microphthalmia, isolated 2, MIM# 610093","entity_name":"VSX2","entity_type":"gene"},{"created":"2022-02-23T16:18:02.131574+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3999","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VSX2 were set to ","entity_name":"VSX2","entity_type":"gene"},{"created":"2022-02-23T16:17:21.290518+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3998","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDPCP as ready","entity_name":"WDPCP","entity_type":"gene"},{"created":"2022-02-23T16:17:21.280961+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3998","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdpcp has been classified as Green List (High Evidence).","entity_name":"WDPCP","entity_type":"gene"},{"created":"2022-02-23T16:17:13.502367+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3998","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDPCP were changed from BARDET-BIEDL SYNDROME TYPE 15 to Bardet-Biedl syndrome 15, MIM# 615992; OFD; Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085","entity_name":"WDPCP","entity_type":"gene"},{"created":"2022-02-23T16:16:59.913387+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3997","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDPCP were set to ","entity_name":"WDPCP","entity_type":"gene"},{"created":"2022-02-23T16:16:07.947480+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3996","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR19 as ready","entity_name":"WDR19","entity_type":"gene"},{"created":"2022-02-23T16:16:07.930024+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3996","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr19 has been classified as Green List (High Evidence).","entity_name":"WDR19","entity_type":"gene"},{"created":"2022-02-23T16:15:49.110847+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3996","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR19 were changed from CRANIOECTODERMAL DYSPLASIA 4; ASPHYXIATING THORACIC DYSTROPHY 5 to Nephronophthisis 13, MIM# 614377; Senior-Loken syndrome 8, MIM# 616307; Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376; Cranioectodermal dysplasia 4, MIM# 614378","entity_name":"WDR19","entity_type":"gene"},{"created":"2022-02-23T16:15:14.633951+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3995","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR19 were set to ","entity_name":"WDR19","entity_type":"gene"},{"created":"2022-02-23T16:14:55.676978+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3994","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Variants in this gene are associated with a range of ciliopathies. Two families reported with a predominantly skeletal phenotype.; to: Variants in this gene are associated with a range of ciliopathies. ","entity_name":"WDR19","entity_type":"gene"},{"created":"2022-02-23T16:14:45.867351+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3994","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: WDR19: Changed rating: GREEN; Changed publications: 33946315, 33875766, 33606107, 22019273, 23559409, 23683095, 32055034; Changed phenotypes: Nephronophthisis 13, MIM# 614377, Senior-Loken syndrome 8, MIM# 616307, Short-rib thoracic dysplasia 5 with or without polydactyly, MIM# 614376, Cranioectodermal dysplasia 4, MIM# 614378","entity_name":"WDR19","entity_type":"gene"},{"created":"2022-02-23T15:51:03.440889+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3994","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBC1D1 as ready","entity_name":"TBC1D1","entity_type":"gene"},{"created":"2022-02-23T15:51:03.431789+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3994","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbc1d1 has been classified as Green List (High Evidence).","entity_name":"TBC1D1","entity_type":"gene"},{"created":"2022-02-23T15:50:57.095295+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3994","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TBC1D1 as Green List (high evidence)","entity_name":"TBC1D1","entity_type":"gene"},{"created":"2022-02-23T15:50:57.085233+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3994","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbc1d1 has been classified as Green List (High Evidence).","entity_name":"TBC1D1","entity_type":"gene"},{"created":"2022-02-23T15:50:20.923122+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3993","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SRGAP1 as ready","entity_name":"SRGAP1","entity_type":"gene"},{"created":"2022-02-23T15:50:20.901183+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3993","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: srgap1 has been classified as Amber List (Moderate Evidence).","entity_name":"SRGAP1","entity_type":"gene"},{"created":"2022-02-23T15:50:13.426904+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3993","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SRGAP1 as Amber List (moderate evidence)","entity_name":"SRGAP1","entity_type":"gene"},{"created":"2022-02-23T15:50:13.417424+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3993","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: srgap1 has been classified as Amber List (Moderate Evidence).","entity_name":"SRGAP1","entity_type":"gene"},{"created":"2022-02-23T15:49:44.492298+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3992","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLIT2 as ready","entity_name":"SLIT2","entity_type":"gene"},{"created":"2022-02-23T15:49:44.479840+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3992","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slit2 has been classified as Amber List (Moderate Evidence).","entity_name":"SLIT2","entity_type":"gene"}]}