{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1700","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1698","results":[{"created":"2020-07-30T19:52:04.354314+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RET as ready","entity_name":"RET","entity_type":"gene"},{"created":"2020-07-30T19:52:04.344046+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ret has been classified as Green List (High Evidence).","entity_name":"RET","entity_type":"gene"},{"created":"2020-07-30T19:51:57.734223+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RET were changed from  to Multiple endocrine neoplasia IIA, MIM# 171400; Multiple endocrine neoplasia IIB, MIM# 162300","entity_name":"RET","entity_type":"gene"},{"created":"2020-07-30T19:51:44.280479+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RET was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RET","entity_type":"gene"},{"created":"2020-07-30T19:51:27.432955+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RET: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Multiple endocrine neoplasia IIA, MIM# 171400, Multiple endocrine neoplasia IIB, MIM# 162300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RET","entity_type":"gene"},{"created":"2020-07-30T19:50:43.999361+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PTEN as ready","entity_name":"PTEN","entity_type":"gene"},{"created":"2020-07-30T19:50:43.990993+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pten has been classified as Green List (High Evidence).","entity_name":"PTEN","entity_type":"gene"},{"created":"2020-07-30T19:50:39.442762+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PTEN were changed from  to Cowden syndrome 1, MIM# 158350","entity_name":"PTEN","entity_type":"gene"},{"created":"2020-07-30T19:50:28.518255+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PTEN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)","entity_name":"PTEN","entity_type":"gene"},{"created":"2020-07-30T19:50:13.832675+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PTEN: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cowden syndrome 1, MIM# 158350; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PTEN","entity_type":"gene"},{"created":"2020-07-30T19:49:43.334921+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKAG2 as ready","entity_name":"PRKAG2","entity_type":"gene"},{"created":"2020-07-30T19:49:43.326891+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkag2 has been classified as Green List (High Evidence).","entity_name":"PRKAG2","entity_type":"gene"},{"created":"2020-07-30T19:49:41.323097+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRKAG2 were changed from  to Cardiomyopathy, hypertrophic 6, MIM# 600858","entity_name":"PRKAG2","entity_type":"gene"},{"created":"2020-07-30T19:49:31.307705+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRKAG2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRKAG2","entity_type":"gene"},{"created":"2020-07-30T19:49:21.177848+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRKAG2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, hypertrophic 6, MIM# 600858; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRKAG2","entity_type":"gene"},{"created":"2020-07-30T19:48:30.567766+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PMS2 as ready","entity_name":"PMS2","entity_type":"gene"},{"created":"2020-07-30T19:48:30.558500+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pms2 has been classified as Green List (High Evidence).","entity_name":"PMS2","entity_type":"gene"},{"created":"2020-07-30T19:48:28.421679+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PMS2 were changed from  to Colorectal cancer, hereditary nonpolyposis, type 4, MIM# 614337","entity_name":"PMS2","entity_type":"gene"},{"created":"2020-07-30T19:48:18.705000+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PMS2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PMS2","entity_type":"gene"},{"created":"2020-07-30T19:48:08.827243+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PMS2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Colorectal cancer, hereditary nonpolyposis, type 4, MIM# 614337; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PMS2","entity_type":"gene"},{"created":"2020-07-30T19:47:39.487624+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PKP2 as ready","entity_name":"PKP2","entity_type":"gene"},{"created":"2020-07-30T19:47:39.470466+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pkp2 has been classified as Green List (High Evidence).","entity_name":"PKP2","entity_type":"gene"},{"created":"2020-07-30T19:47:33.823772+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PKP2 were changed from  to Arrhythmogenic right ventricular dysplasia 9, MIM# 609040","entity_name":"PKP2","entity_type":"gene"},{"created":"2020-07-30T19:47:24.337010+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PKP2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PKP2","entity_type":"gene"},{"created":"2020-07-30T19:47:11.409719+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PKP2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Arrhythmogenic right ventricular dysplasia 9, MIM# 609040; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PKP2","entity_type":"gene"},{"created":"2020-07-30T18:57:28.479170+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCSK9 as ready","entity_name":"PCSK9","entity_type":"gene"},{"created":"2020-07-30T18:57:28.468383+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcsk9 has been classified as Green List (High Evidence).","entity_name":"PCSK9","entity_type":"gene"},{"created":"2020-07-30T18:57:26.358405+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCSK9 were changed from  to Hypercholesterolemia, familial, 3, MIM# 603776","entity_name":"PCSK9","entity_type":"gene"},{"created":"2020-07-30T18:57:20.063496+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PCSK9 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PCSK9","entity_type":"gene"},{"created":"2020-07-30T18:57:11.648522+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PCSK9: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypercholesterolemia, familial, 3, MIM# 603776; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PCSK9","entity_type":"gene"},{"created":"2020-07-30T18:56:41.230660+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OTC as ready","entity_name":"OTC","entity_type":"gene"},{"created":"2020-07-30T18:56:41.220876+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: otc has been classified as Green List (High Evidence).","entity_name":"OTC","entity_type":"gene"},{"created":"2020-07-30T18:56:39.416542+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OTC were changed from  to Ornithine transcarbamylase deficiency, MIM# 311250","entity_name":"OTC","entity_type":"gene"},{"created":"2020-07-30T18:56:31.412368+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OTC was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"OTC","entity_type":"gene"},{"created":"2020-07-30T18:56:21.866278+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: OTC: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Ornithine transcarbamylase deficiency, MIM# 311250; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"OTC","entity_type":"gene"},{"created":"2020-07-30T18:55:54.537080+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NF2 as ready","entity_name":"NF2","entity_type":"gene"},{"created":"2020-07-30T18:55:54.525851+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nf2 has been classified as Green List (High Evidence).","entity_name":"NF2","entity_type":"gene"},{"created":"2020-07-30T18:55:52.802273+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NF2 were changed from  to Neurofibromatosis, type 2, MIM# 101000","entity_name":"NF2","entity_type":"gene"},{"created":"2020-07-30T18:55:45.165292+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NF2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NF2","entity_type":"gene"},{"created":"2020-07-30T18:55:36.376402+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NF2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurofibromatosis, type 2, MIM# 101000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NF2","entity_type":"gene"},{"created":"2020-07-30T18:55:10.456580+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYL3 as ready","entity_name":"MYL3","entity_type":"gene"},{"created":"2020-07-30T18:55:10.445982+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myl3 has been classified as Green List (High Evidence).","entity_name":"MYL3","entity_type":"gene"},{"created":"2020-07-30T18:55:07.827178+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYL3 were changed from  to Cardiomyopathy, hypertrophic, 8, MIM# 608751","entity_name":"MYL3","entity_type":"gene"},{"created":"2020-07-30T18:54:50.806944+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYL3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MYL3","entity_type":"gene"},{"created":"2020-07-30T18:54:40.580311+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYL3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, hypertrophic, 8, MIM# 608751; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MYL3","entity_type":"gene"},{"created":"2020-07-30T18:54:04.988139+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYL2 as ready","entity_name":"MYL2","entity_type":"gene"},{"created":"2020-07-30T18:54:04.965185+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myl2 has been classified as Green List (High Evidence).","entity_name":"MYL2","entity_type":"gene"},{"created":"2020-07-30T18:54:03.261283+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYL2 were changed from  to Cardiomyopathy, hypertrophic, 10, MIM# 608758","entity_name":"MYL2","entity_type":"gene"},{"created":"2020-07-30T18:53:53.795212+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYL2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYL2","entity_type":"gene"},{"created":"2020-07-30T18:53:36.812539+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYL2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, hypertrophic, 10, MIM# 608758; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYL2","entity_type":"gene"},{"created":"2020-07-30T18:53:11.965479+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYH7 as ready","entity_name":"MYH7","entity_type":"gene"},{"created":"2020-07-30T18:53:11.957029+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myh7 has been classified as Green List (High Evidence).","entity_name":"MYH7","entity_type":"gene"},{"created":"2020-07-30T18:53:09.838243+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYH7 were changed from  to Cardiomyopathy, dilated, 1S, MIM# 613426; Cardiomyopathy, hypertrophic, 1, MIM# 192600","entity_name":"MYH7","entity_type":"gene"},{"created":"2020-07-30T18:53:02.206327+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYH7 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYH7","entity_type":"gene"},{"created":"2020-07-30T18:52:52.321009+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYH7: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, dilated, 1S, MIM# 613426, Cardiomyopathy, hypertrophic, 1, MIM# 192600; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYH7","entity_type":"gene"},{"created":"2020-07-30T18:52:17.782459+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYH11 as ready","entity_name":"MYH11","entity_type":"gene"},{"created":"2020-07-30T18:52:17.774281+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myh11 has been classified as Green List (High Evidence).","entity_name":"MYH11","entity_type":"gene"},{"created":"2020-07-30T18:52:15.975626+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYH11 were changed from  to Aortic aneurysm, familial thoracic 4, MIM# 132900","entity_name":"MYH11","entity_type":"gene"},{"created":"2020-07-30T18:52:09.137189+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYH11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYH11","entity_type":"gene"},{"created":"2020-07-30T18:52:00.008079+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYH11: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aortic aneurysm, familial thoracic 4, MIM# 132900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYH11","entity_type":"gene"},{"created":"2020-07-30T18:51:33.263837+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYBPC3 as ready","entity_name":"MYBPC3","entity_type":"gene"},{"created":"2020-07-30T18:51:33.255388+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mybpc3 has been classified as Green List (High Evidence).","entity_name":"MYBPC3","entity_type":"gene"},{"created":"2020-07-30T18:51:31.486431+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYBPC3 were changed from  to Cardiomyopathy, dilated, 1MM, MIM# 615396; Cardiomyopathy, hypertrophic, 4, MIM# 115197; Left ventricular noncompaction 10, MIM# 615396","entity_name":"MYBPC3","entity_type":"gene"},{"created":"2020-07-30T18:51:24.674076+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYBPC3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MYBPC3","entity_type":"gene"},{"created":"2020-07-30T18:51:13.495353+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYBPC3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, dilated, 1MM, MIM# 615396, Cardiomyopathy, hypertrophic, 4, MIM# 115197, Left ventricular noncompaction 10, MIM# 615396; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MYBPC3","entity_type":"gene"},{"created":"2020-07-30T18:50:27.730766+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MUTYH as ready","entity_name":"MUTYH","entity_type":"gene"},{"created":"2020-07-30T18:50:27.721018+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mutyh has been classified as Green List (High Evidence).","entity_name":"MUTYH","entity_type":"gene"},{"created":"2020-07-30T18:50:25.929153+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MUTYH were changed from  to Adenomas, multiple colorectal, MIM# 608456","entity_name":"MUTYH","entity_type":"gene"},{"created":"2020-07-30T18:50:12.825259+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MUTYH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MUTYH","entity_type":"gene"},{"created":"2020-07-30T18:50:03.200019+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MUTYH: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Adenomas, multiple colorectal, MIM# 608456; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MUTYH","entity_type":"gene"},{"created":"2020-07-30T18:28:46.033932+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MSH6 as ready","entity_name":"MSH6","entity_type":"gene"},{"created":"2020-07-30T18:28:46.023515+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: msh6 has been classified as Green List (High Evidence).","entity_name":"MSH6","entity_type":"gene"},{"created":"2020-07-30T18:28:43.554986+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MSH6 were changed from  to Colorectal cancer, hereditary nonpolyposis, type 5, MIM# 614350","entity_name":"MSH6","entity_type":"gene"},{"created":"2020-07-30T18:28:35.232330+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MSH6 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MSH6","entity_type":"gene"},{"created":"2020-07-30T18:28:25.759292+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MSH6: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Colorectal cancer, hereditary nonpolyposis, type 5, MIM# 614350; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MSH6","entity_type":"gene"},{"created":"2020-07-30T18:27:59.012166+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MSH2 as ready","entity_name":"MSH2","entity_type":"gene"},{"created":"2020-07-30T18:27:59.004328+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: msh2 has been classified as Green List (High Evidence).","entity_name":"MSH2","entity_type":"gene"},{"created":"2020-07-30T18:27:57.178123+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MSH2 were changed from  to Colorectal cancer, hereditary nonpolyposis, type 1, MIM# 120435","entity_name":"MSH2","entity_type":"gene"},{"created":"2020-07-30T18:27:45.115004+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MSH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MSH2","entity_type":"gene"},{"created":"2020-07-30T18:27:35.351674+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MSH2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Colorectal cancer, hereditary nonpolyposis, type 1, MIM# 120435; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MSH2","entity_type":"gene"},{"created":"2020-07-30T18:27:04.839386+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MLH1 as ready","entity_name":"MLH1","entity_type":"gene"},{"created":"2020-07-30T18:27:04.830683+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mlh1 has been classified as Green List (High Evidence).","entity_name":"MLH1","entity_type":"gene"},{"created":"2020-07-30T18:27:02.441752+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MLH1 were changed from  to Colorectal cancer, hereditary nonpolyposis, type 2, MIM# 609310","entity_name":"MLH1","entity_type":"gene"},{"created":"2020-07-30T18:26:54.725206+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MLH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MLH1","entity_type":"gene"},{"created":"2020-07-30T18:26:45.959296+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MLH1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Colorectal cancer, hereditary nonpolyposis, type 2, MIM# 609310; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MLH1","entity_type":"gene"},{"created":"2020-07-30T18:26:15.451132+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MEN1 as ready","entity_name":"MEN1","entity_type":"gene"},{"created":"2020-07-30T18:26:15.443256+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: men1 has been classified as Green List (High Evidence).","entity_name":"MEN1","entity_type":"gene"},{"created":"2020-07-30T18:26:12.110673+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MEN1 were changed from  to Multiple endocrine neoplasia 1, MIM# 131100","entity_name":"MEN1","entity_type":"gene"},{"created":"2020-07-30T18:26:05.442042+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MEN1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MEN1","entity_type":"gene"},{"created":"2020-07-30T18:25:56.423396+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MEN1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Multiple endocrine neoplasia 1, MIM# 131100; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MEN1","entity_type":"gene"},{"created":"2020-07-30T18:25:31.519424+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LMNA as ready","entity_name":"LMNA","entity_type":"gene"},{"created":"2020-07-30T18:25:31.510431+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lmna has been classified as Green List (High Evidence).","entity_name":"LMNA","entity_type":"gene"},{"created":"2020-07-30T18:25:29.506050+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LMNA were changed from  to Cardiomyopathy, dilated, 1A, MIM# 115200","entity_name":"LMNA","entity_type":"gene"},{"created":"2020-07-30T18:25:10.169175+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LMNA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LMNA","entity_type":"gene"},{"created":"2020-07-30T18:25:01.896259+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LMNA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cardiomyopathy, dilated, 1A, MIM# 115200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LMNA","entity_type":"gene"},{"created":"2020-07-30T18:24:33.486053+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LDLR as ready","entity_name":"LDLR","entity_type":"gene"},{"created":"2020-07-30T18:24:33.478041+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ldlr has been classified as Green List (High Evidence).","entity_name":"LDLR","entity_type":"gene"},{"created":"2020-07-30T18:24:31.365023+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LDLR were changed from  to Hypercholesterolemia, familial, 1, MIM# 143890","entity_name":"LDLR","entity_type":"gene"},{"created":"2020-07-30T18:24:19.376946+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LDLR was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LDLR","entity_type":"gene"},{"created":"2020-07-30T18:24:10.790243+10:00","panel_name":"Additional findings_Adult","panel_id":221,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LDLR: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypercholesterolemia, familial, 1, MIM# 143890; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LDLR","entity_type":"gene"}]}