{"count":220751,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=975","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=973","results":[{"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"},{"created":"2022-02-23T15:49:37.489836+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3992","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLIT2 as Amber List (moderate evidence)","entity_name":"SLIT2","entity_type":"gene"},{"created":"2022-02-23T15:49:37.478398+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"},{"created":"2022-02-23T15:49:09.748912+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3991","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ANKRD17 as ready","entity_name":"ANKRD17","entity_type":"gene"},{"created":"2022-02-23T15:49:09.733681+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3991","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ankrd17 has been classified as Green List (High Evidence).","entity_name":"ANKRD17","entity_type":"gene"},{"created":"2022-02-23T15:49:02.485974+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3991","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ANKRD17 as Green List (high evidence)","entity_name":"ANKRD17","entity_type":"gene"},{"created":"2022-02-23T15:49:02.465853+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3991","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ankrd17 has been classified as Green List (High Evidence).","entity_name":"ANKRD17","entity_type":"gene"},{"created":"2022-02-23T15:48:35.971431+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3990","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALB as ready","entity_name":"ALB","entity_type":"gene"},{"created":"2022-02-23T15:48:35.959607+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3990","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alb has been classified as Green List (High Evidence).","entity_name":"ALB","entity_type":"gene"},{"created":"2022-02-23T15:48:29.886840+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3990","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ALB as Green List (high evidence)","entity_name":"ALB","entity_type":"gene"},{"created":"2022-02-23T15:48:29.874578+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3990","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alb has been classified as Green List (High Evidence).","entity_name":"ALB","entity_type":"gene"},{"created":"2022-02-23T15:47:50.877082+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3989","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACBD5 as ready","entity_name":"ACBD5","entity_type":"gene"},{"created":"2022-02-23T15:47:50.867298+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3989","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acbd5 has been classified as Red List (Low Evidence).","entity_name":"ACBD5","entity_type":"gene"},{"created":"2022-02-23T15:47:43.885781+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3989","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ACBD5 as Red List (low evidence)","entity_name":"ACBD5","entity_type":"gene"},{"created":"2022-02-23T15:47:43.876271+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3989","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: acbd5 has been classified as Red List (Low Evidence).","entity_name":"ACBD5","entity_type":"gene"},{"created":"2022-02-23T15:46:53.908558+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3988","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF711 as ready","entity_name":"ZNF711","entity_type":"gene"},{"created":"2022-02-23T15:46:53.897730+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3988","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf711 has been classified as Red List (Low Evidence).","entity_name":"ZNF711","entity_type":"gene"},{"created":"2022-02-23T15:46:47.376595+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3988","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF711 were changed from MENTAL RETARDATION X-LINKED ZNF711-RELATED to Mental retardation, X-linked 97, OMIM #300803","entity_name":"ZNF711","entity_type":"gene"},{"created":"2022-02-23T15:46:29.252898+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3987","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZNF711 were set to ","entity_name":"ZNF711","entity_type":"gene"},{"created":"2022-02-23T15:46:12.992439+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3986","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZNF711: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation, X-linked 97, OMIM #300803; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"ZNF711","entity_type":"gene"},{"created":"2022-02-23T15:45:12.330103+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3986","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF3 as ready","entity_name":"ZNF3","entity_type":"gene"},{"created":"2022-02-23T15:45:12.308018+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3986","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf3 has been classified as Red List (Low Evidence).","entity_name":"ZNF3","entity_type":"gene"},{"created":"2022-02-23T15:43:57.129836+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3986","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: XPA as ready","entity_name":"XPA","entity_type":"gene"},{"created":"2022-02-23T15:43:57.117888+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3986","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: xpa has been classified as Red List (Low Evidence).","entity_name":"XPA","entity_type":"gene"},{"created":"2022-02-23T15:43:52.921188+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3986","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: XPA were changed from XERODERMA PIGMENTOSUM, GROUP A to Xeroderma pigmentosum, group A, OMIM# 278700","entity_name":"XPA","entity_type":"gene"},{"created":"2022-02-23T15:43:39.408808+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3985","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: XPA were set to ","entity_name":"XPA","entity_type":"gene"},{"created":"2022-02-23T15:43:23.672323+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3984","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Multiple families reported where ID is part of the phenotype, though some share haplotype and are likely distantly related.; to: Clinical presentation is typically post-natal.","entity_name":"XPA","entity_type":"gene"},{"created":"2022-02-23T15:43:09.897798+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3984","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: XPA: Changed rating: RED","entity_name":"XPA","entity_type":"gene"},{"created":"2022-02-23T15:42:43.233871+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3984","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR91 as ready","entity_name":"WDR91","entity_type":"gene"},{"created":"2022-02-23T15:42:43.223836+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3984","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr91 has been classified as Amber List (Moderate Evidence).","entity_name":"WDR91","entity_type":"gene"},{"created":"2022-02-23T15:42:36.012941+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3984","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: WDR91 as Amber List (moderate evidence)","entity_name":"WDR91","entity_type":"gene"},{"created":"2022-02-23T15:42:35.993500+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3984","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr91 has been classified as Amber List (Moderate Evidence).","entity_name":"WDR91","entity_type":"gene"},{"created":"2022-02-23T15:41:59.389837+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3983","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR11 as ready","entity_name":"WDR11","entity_type":"gene"},{"created":"2022-02-23T15:41:59.379553+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3983","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr11 has been classified as Amber List (Moderate Evidence).","entity_name":"WDR11","entity_type":"gene"},{"created":"2022-02-23T15:41:54.271582+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3983","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR11 were changed from KALLMANN SYNDROME to Intellectual disability; Microcephaly; Short stature","entity_name":"WDR11","entity_type":"gene"},{"created":"2022-02-23T15:41:40.203398+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3982","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR11 were set to ","entity_name":"WDR11","entity_type":"gene"},{"created":"2022-02-23T15:41:27.273468+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3981","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR11 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR11","entity_type":"gene"},{"created":"2022-02-23T15:41:16.108853+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3980","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: WDR11 as Amber List (moderate evidence)","entity_name":"WDR11","entity_type":"gene"},{"created":"2022-02-23T15:41:16.091892+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.3980","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr11 has been classified as Amber List (Moderate Evidence).","entity_name":"WDR11","entity_type":"gene"}]}