{"count":220959,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1023","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1021","results":[{"created":"2022-01-25T18:47:40.365678+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2816","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tspan7 has been classified as Red List (Low Evidence).","entity_name":"TSPAN7","entity_type":"gene"},{"created":"2022-01-25T18:47:34.949886+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2816","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSPAN7 were changed from MENTAL RETARDATION X-LINKED TYPE 58 to Intellectual developmental disorder, X-linked 58, MIM# 300210","entity_name":"TSPAN7","entity_type":"gene"},{"created":"2022-01-25T18:47:18.591553+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2815","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TSPAN7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Intellectual developmental disorder, X-linked 58, MIM# 300210; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"TSPAN7","entity_type":"gene"},{"created":"2022-01-25T18:44:11.573768+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2815","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:TRAPPC2 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-25T18:43:27.161672+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2814","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:TPP1 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-25T18:42:10.189951+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2813","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TOGARAM1 as ready","entity_name":"TOGARAM1","entity_type":"gene"},{"created":"2022-01-25T18:42:10.178611+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2813","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: togaram1 has been classified as Red List (Low Evidence).","entity_name":"TOGARAM1","entity_type":"gene"},{"created":"2022-01-25T18:41:44.783377+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2813","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:TMPRSS6 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-25T18:40:58.720280+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2812","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:TNFRSF11B from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-25T18:40:07.455547+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2811","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:TNFRSF13B from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-25T18:38:10.776266+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2810","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MEGF8 as ready","entity_name":"MEGF8","entity_type":"gene"},{"created":"2022-01-25T18:38:10.765624+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2810","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: megf8 has been classified as Green List (High Evidence).","entity_name":"MEGF8","entity_type":"gene"},{"created":"2022-01-25T18:36:21.224296+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2810","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MEGF8 were changed from CARPENTER SYNDROME to Carpenter syndrome 2, MIM #614976","entity_name":"MEGF8","entity_type":"gene"},{"created":"2022-01-25T18:36:04.839934+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2809","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MEGF8 were set to ","entity_name":"MEGF8","entity_type":"gene"},{"created":"2022-01-25T18:35:51.196357+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2808","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: ID is described in this condition. \nSources: Expert list; to: Craniosynostosis and polysyndactyly.\r\n\r\n\r\nSources: Expert list","entity_name":"MEGF8","entity_type":"gene"},{"created":"2022-01-25T18:34:49.880249+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2808","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MEF2C as ready","entity_name":"MEF2C","entity_type":"gene"},{"created":"2022-01-25T18:34:49.868609+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2808","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mef2c has been classified as Green List (High Evidence).","entity_name":"MEF2C","entity_type":"gene"},{"created":"2022-01-25T18:34:45.518631+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2808","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MEF2C were changed from MENTAL RETARDATION-STEREOTYPIC MOVEMENTS-EPILEPSY AND/OR CEREBRAL MALFORMATIONS to Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations, MIM# 613443; MONDO:0013266","entity_name":"MEF2C","entity_type":"gene"},{"created":"2022-01-25T18:34:31.788704+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2807","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MEF2C were set to ","entity_name":"MEF2C","entity_type":"gene"},{"created":"2022-01-25T18:34:12.018036+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2806","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MEF2C was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MEF2C","entity_type":"gene"},{"created":"2022-01-25T18:34:00.657036+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2805","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: MEF2C.","entity_name":"MEF2C","entity_type":"gene"},{"created":"2022-01-25T18:33:27.012957+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2805","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MED12 as ready","entity_name":"MED12","entity_type":"gene"},{"created":"2022-01-25T18:33:27.000835+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2805","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: med12 has been classified as Green List (High Evidence).","entity_name":"MED12","entity_type":"gene"},{"created":"2022-01-25T18:33:23.799775+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2805","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MED12 were changed from LUJAN-FRYNS SYNDROME; OPITZ-KAVEGGIA SYNDROME to Lujan-Fryns syndrome, MIM#\t309520; Opitz-Kaveggia syndrome, MIM#\t305450","entity_name":"MED12","entity_type":"gene"},{"created":"2022-01-25T18:32:39.867560+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2804","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MED12 were set to ","entity_name":"MED12","entity_type":"gene"},{"created":"2022-01-25T18:31:46.703174+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2803","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MCPH1 as ready","entity_name":"MCPH1","entity_type":"gene"},{"created":"2022-01-25T18:31:46.691519+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2803","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcph1 has been classified as Green List (High Evidence).","entity_name":"MCPH1","entity_type":"gene"},{"created":"2022-01-25T18:31:43.358787+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2803","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MCPH1 were changed from MICROCEPHALY PRIMARY TYPE 1 to Microcephaly 1, primary, autosomal recessive, MIM# 251200","entity_name":"MCPH1","entity_type":"gene"},{"created":"2022-01-25T18:31:30.509185+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2802","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MCPH1 were set to ","entity_name":"MCPH1","entity_type":"gene"},{"created":"2022-01-25T18:31:16.340239+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2801","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established primary micorcephaly gene.\r\n\r\nSources: Literature; to: Well established primary microcephaly gene.\r\n\r\nSources: Literature","entity_name":"MCPH1","entity_type":"gene"},{"created":"2022-01-25T18:31:07.307407+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2801","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Single individual reported as part of a CDH cohort. \nSources: Literature; to: Well established primary micorcephaly gene.\r\n\r\nSources: Literature","entity_name":"MCPH1","entity_type":"gene"},{"created":"2022-01-25T18:30:48.770512+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2801","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: MCPH1: Changed rating: GREEN; Changed phenotypes: Microcephaly 1, primary, autosomal recessive, MIM# 251200","entity_name":"MCPH1","entity_type":"gene"},{"created":"2022-01-25T18:30:15.957265+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2801","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MCOLN1 as ready","entity_name":"MCOLN1","entity_type":"gene"},{"created":"2022-01-25T18:30:15.944674+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2801","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcoln1 has been classified as Green List (High Evidence).","entity_name":"MCOLN1","entity_type":"gene"},{"created":"2022-01-25T18:30:09.629315+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2801","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MCOLN1 were changed from MUCOLIPIDOSIS IV to Mucolipidosis IV, MIM# 252650; MONDO:0009653","entity_name":"MCOLN1","entity_type":"gene"},{"created":"2022-01-25T18:29:57.858255+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2800","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MCOLN1 were set to ","entity_name":"MCOLN1","entity_type":"gene"},{"created":"2022-01-25T18:29:42.905913+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2799","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: MCOLN1: Added comment: Prenatal presentations with brain abnormalities reported.; Changed rating: GREEN; Changed publications: 33963976","entity_name":"MCOLN1","entity_type":"gene"},{"created":"2022-01-25T18:28:48.171245+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2799","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: MCOLN1: Changed rating: RED","entity_name":"MCOLN1","entity_type":"gene"},{"created":"2022-01-25T18:27:51.693441+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2799","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MATN3 as ready","entity_name":"MATN3","entity_type":"gene"},{"created":"2022-01-25T18:27:51.683072+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2799","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: matn3 has been classified as Green List (High Evidence).","entity_name":"MATN3","entity_type":"gene"},{"created":"2022-01-25T18:27:47.984710+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2799","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MATN3 were changed from Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type (MIM#608728); Epiphyseal dysplasia, multiple, 5 (MIM#607078) to Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type, MIM# 608728","entity_name":"MATN3","entity_type":"gene"},{"created":"2022-01-25T18:27:28.222707+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2798","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MATN3 was changed from BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MATN3","entity_type":"gene"},{"created":"2022-01-25T18:27:10.158809+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2797","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MATN3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type, MIM# 608728; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MATN3","entity_type":"gene"},{"created":"2022-01-25T18:25:19.821435+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2797","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MASP1 as ready","entity_name":"MASP1","entity_type":"gene"},{"created":"2022-01-25T18:25:19.809500+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2797","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: masp1 has been classified as Green List (High Evidence).","entity_name":"MASP1","entity_type":"gene"},{"created":"2022-01-25T18:25:15.770388+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2797","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MASP1 were changed from 3MC SYNDROME 1 to 3MC syndrome 1, MIM# 257920; MONDO:0009770","entity_name":"MASP1","entity_type":"gene"},{"created":"2022-01-25T18:25:03.581240+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2796","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MASP1 were set to ","entity_name":"MASP1","entity_type":"gene"},{"created":"2022-01-25T18:24:26.580951+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2795","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAPRE2 as ready","entity_name":"MAPRE2","entity_type":"gene"},{"created":"2022-01-25T18:24:26.568434+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2795","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mapre2 has been classified as Green List (High Evidence).","entity_name":"MAPRE2","entity_type":"gene"},{"created":"2022-01-25T18:24:23.084438+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2795","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAPRE2 were changed from Symmetric circumferential skin creases, congenital, 2, 616734 to Symmetric circumferential skin creases, congenital, 2, MIM#616734","entity_name":"MAPRE2","entity_type":"gene"},{"created":"2022-01-25T18:24:07.642244+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2794","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MAPRE2 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"MAPRE2","entity_type":"gene"},{"created":"2022-01-25T18:23:54.042120+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2793","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: ID is part of the phenotype, more severe in those with bi-allelic variants. \nSources: Expert list; to: Cleft palate and microcephaly reported.\r\n\r\nSources: Expert list","entity_name":"MAPRE2","entity_type":"gene"},{"created":"2022-01-25T18:18:36.625059+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2793","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAP2K2 as ready","entity_name":"MAP2K2","entity_type":"gene"},{"created":"2022-01-25T18:18:36.614108+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2793","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: map2k2 has been classified as Green List (High Evidence).","entity_name":"MAP2K2","entity_type":"gene"},{"created":"2022-01-25T18:18:32.869558+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2793","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAP2K2 were changed from CARDIOFACIOCUTANEOUS SYNDROME to Cardiofaciocutaneous syndrome 4, MIM# 615280","entity_name":"MAP2K2","entity_type":"gene"},{"created":"2022-01-25T18:18:18.726873+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2792","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MAP2K2 were set to ","entity_name":"MAP2K2","entity_type":"gene"},{"created":"2022-01-25T18:18:07.082792+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2791","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: MAP2K2 was changed from  to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"MAP2K2","entity_type":"gene"},{"created":"2022-01-25T18:17:57.129939+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2790","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MAP2K2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MAP2K2","entity_type":"gene"},{"created":"2022-01-25T18:17:29.260457+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2789","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAP2K1 as ready","entity_name":"MAP2K1","entity_type":"gene"},{"created":"2022-01-25T18:17:29.249807+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2789","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: map2k1 has been classified as Green List (High Evidence).","entity_name":"MAP2K1","entity_type":"gene"},{"created":"2022-01-25T18:17:25.679699+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2789","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAP2K1 were changed from CARDIOFACIOCUTANEOUS SYNDROME to Cardiofaciocutaneous syndrome 3, MIM# 615279","entity_name":"MAP2K1","entity_type":"gene"},{"created":"2022-01-25T18:17:13.429330+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2788","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MAP2K1 were set to ","entity_name":"MAP2K1","entity_type":"gene"},{"created":"2022-01-25T18:17:00.763818+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2787","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: MAP2K1 was changed from  to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"MAP2K1","entity_type":"gene"},{"created":"2022-01-25T18:16:49.909411+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2786","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MAP2K1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MAP2K1","entity_type":"gene"},{"created":"2022-01-25T18:16:09.679436+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2785","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAGEL2 as ready","entity_name":"MAGEL2","entity_type":"gene"},{"created":"2022-01-25T18:16:09.669146+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2785","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: magel2 has been classified as Green List (High Evidence).","entity_name":"MAGEL2","entity_type":"gene"},{"created":"2022-01-25T18:16:05.762080+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2785","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAGEL2 were changed from ARTHROGRYPOSIS MULTIPLEX CONGENITA; Schaaf-Yang syndrome, 615547; Schaaf-Yang syndrome to Schaaf-Yang syndrome, MIM# 615547","entity_name":"MAGEL2","entity_type":"gene"},{"created":"2022-01-25T18:15:50.829015+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2784","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MAGEL2 were set to 26365340; 27195816","entity_name":"MAGEL2","entity_type":"gene"},{"created":"2022-01-25T18:15:00.335234+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2783","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAB21L2 as ready","entity_name":"MAB21L2","entity_type":"gene"},{"created":"2022-01-25T18:15:00.322668+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2783","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mab21l2 has been classified as Green List (High Evidence).","entity_name":"MAB21L2","entity_type":"gene"},{"created":"2022-01-25T18:14:55.933152+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2783","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAB21L2 were changed from MICROPHTHALMIA, SYNDROMIC 14 to Microphthalmia/coloboma and skeletal dysplasia syndrome, MIM# 615877","entity_name":"MAB21L2","entity_type":"gene"},{"created":"2022-01-25T18:14:42.731614+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2782","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MAB21L2 were set to ","entity_name":"MAB21L2","entity_type":"gene"},{"created":"2022-01-25T18:13:58.421278+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2781","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LZTR1 as ready","entity_name":"LZTR1","entity_type":"gene"},{"created":"2022-01-25T18:13:58.410214+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2781","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lztr1 has been classified as Green List (High Evidence).","entity_name":"LZTR1","entity_type":"gene"},{"created":"2022-01-25T18:13:54.501107+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2781","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LZTR1 were changed from Noonan syndrome 10, 616564; Fetal hydrops to Noonan syndrome 10, MIM#616564; Noonan syndrome 2, MIM#605275; Fetal hydrops","entity_name":"LZTR1","entity_type":"gene"},{"created":"2022-01-25T18:13:38.421063+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2780","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: LZTR1 was changed from  to Other","entity_name":"LZTR1","entity_type":"gene"},{"created":"2022-01-25T18:13:29.330101+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2779","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LZTR1 were set to ","entity_name":"LZTR1","entity_type":"gene"},{"created":"2022-01-25T18:12:51.484194+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2778","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LZTFL1 as ready","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2022-01-25T18:12:51.474029+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2778","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lztfl1 has been classified as Green List (High Evidence).","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2022-01-25T18:12:48.043157+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2778","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LZTFL1 were changed from Bardet-Biedl syndrome 17 615994 to Bardet-Biedl syndrome 17, MIM# 615994","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2022-01-25T18:12:35.786959+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2777","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LZTFL1 were set to ","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2022-01-25T18:12:16.378743+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2776","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2022-01-25T18:11:38.035804+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2776","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LYST as ready","entity_name":"LYST","entity_type":"gene"},{"created":"2022-01-25T18:11:38.025285+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2776","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lyst has been classified as Red List (Low Evidence).","entity_name":"LYST","entity_type":"gene"},{"created":"2022-01-25T18:11:33.789091+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2776","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LYST were changed from CHEDIAK-HIGASHI SYNDROME to Chediak-Higashi syndrome, MIM#214500","entity_name":"LYST","entity_type":"gene"},{"created":"2022-01-25T18:11:20.838359+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2775","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LYST as Red List (low evidence)","entity_name":"LYST","entity_type":"gene"},{"created":"2022-01-25T18:11:20.825485+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2775","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lyst has been classified as Red List (Low Evidence).","entity_name":"LYST","entity_type":"gene"},{"created":"2022-01-25T18:10:39.155078+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2774","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: LYST: Presentation is typically post-natal.","entity_name":"LYST","entity_type":"gene"},{"created":"2022-01-25T18:10:27.919919+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2774","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: LYST: Changed rating: RED","entity_name":"LYST","entity_type":"gene"},{"created":"2022-01-25T18:09:38.456416+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2774","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"LYST","entity_type":"gene"},{"created":"2022-01-25T18:09:35.379052+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2774","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"LYST","entity_type":"gene"},{"created":"2022-01-25T18:09:05.016615+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2774","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRRC6 as ready","entity_name":"LRRC6","entity_type":"gene"},{"created":"2022-01-25T18:09:05.006424+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2774","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrrc6 has been classified as Green List (High Evidence).","entity_name":"LRRC6","entity_type":"gene"},{"created":"2022-01-25T18:09:00.402041+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2774","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRRC6 were changed from PRIMARY CILIARY DISKINESIA to Ciliary dyskinesia, primary, 19, MIM# 614935","entity_name":"LRRC6","entity_type":"gene"},{"created":"2022-01-25T18:08:45.452028+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2773","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LRRC6 were set to ","entity_name":"LRRC6","entity_type":"gene"},{"created":"2022-01-25T18:08:27.958210+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2772","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: More than 10 unrelated families reported.; to: More than 10 unrelated families reported. Situs inversus is a feature.","entity_name":"LRRC6","entity_type":"gene"},{"created":"2022-01-25T18:07:36.149028+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2772","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRP5 as ready","entity_name":"LRP5","entity_type":"gene"},{"created":"2022-01-25T18:07:36.136699+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2772","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrp5 has been classified as Green List (High Evidence).","entity_name":"LRP5","entity_type":"gene"},{"created":"2022-01-25T18:07:32.304256+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2772","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRP5 were changed from HIGH BONE MASS TRAIT; ENDOSTEAL HYPEROSTOSIS WORTH TYPE; VITREORETINOPATHY EXUDATIVE TYPE 4; OSTEOPETROSIS AUTOSOMAL DOMINANT TYPE 1; OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME to Osteoporosis-pseudoglioma syndrome, MIM# 259770; Polycystic liver disease 4 with or without kidney cysts, MIM# 617875","entity_name":"LRP5","entity_type":"gene"},{"created":"2022-01-25T18:07:16.477189+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2771","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LRP5 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"LRP5","entity_type":"gene"}]}