{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=924","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=922","results":[{"created":"2022-03-22T12:34:20.942487+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11715","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ACP4 were changed from  to Amelogenesis imperfecta, type IJ MIM#617297","entity_name":"ACP4","entity_type":"gene"},{"created":"2022-03-22T12:34:17.398477+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11715","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: ACP4 were set to ","entity_name":"ACP4","entity_type":"gene"},{"created":"2022-03-22T12:34:06.092441+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11714","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ACP4 as ready","entity_name":"ACP4","entity_type":"gene"},{"created":"2022-03-22T12:34:06.029783+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11714","user_name":"Elena Savva","item_type":"entity","text":"Gene: acp4 has been classified as Green List (High Evidence).","entity_name":"ACP4","entity_type":"gene"},{"created":"2022-03-22T12:33:55.852304+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11714","user_name":"Elena Savva","item_type":"entity","text":"Mode of inheritance for gene: ACP4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACP4","entity_type":"gene"},{"created":"2022-03-22T12:33:19.438143+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11713","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: ACHE were set to ","entity_name":"ACHE","entity_type":"gene"},{"created":"2022-03-22T12:33:18.177098+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11713","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ACHE were changed from  to [Blood group, Yt system] MIM#112100","entity_name":"ACHE","entity_type":"gene"},{"created":"2022-03-22T12:33:07.221221+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11712","user_name":"Elena Savva","item_type":"entity","text":"Classified gene: ACHE as Red List (low evidence)","entity_name":"ACHE","entity_type":"gene"},{"created":"2022-03-22T12:33:07.208433+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11712","user_name":"Elena Savva","item_type":"entity","text":"Gene: ache has been classified as Red List (Low Evidence).","entity_name":"ACHE","entity_type":"gene"},{"created":"2022-03-22T12:30:28.997770+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11711","user_name":"Elena Savva","item_type":"entity","text":"reviewed gene: ACHE: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 12783426, 8488842; Phenotypes: [Blood group, Yt system] MIM#112100; Mode of inheritance: Unknown","entity_name":"ACHE","entity_type":"gene"},{"created":"2022-03-22T12:16:34.870534+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11711","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ACADSB were changed from  to 2-methylbutyrylglycinuria MIM#610006","entity_name":"ACADSB","entity_type":"gene"},{"created":"2022-03-22T12:02:05.793621+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11710","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UNG was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"UNG","entity_type":"gene"},{"created":"2022-03-22T11:57:29.356750+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11709","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: ACADSB were set to ","entity_name":"ACADSB","entity_type":"gene"},{"created":"2022-03-22T11:57:24.162199+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11709","user_name":"Elena Savva","item_type":"entity","text":"Mode of inheritance for gene: ACADSB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACADSB","entity_type":"gene"},{"created":"2022-03-22T11:57:04.640193+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11708","user_name":"Elena Savva","item_type":"entity","text":"reviewed gene: ACADSB: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 25778941, 17945527; Phenotypes: 2-methylbutyrylglycinuria MIM#610006; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACADSB","entity_type":"gene"},{"created":"2022-03-22T10:54:32.154957+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11708","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WAS as ready","entity_name":"WAS","entity_type":"gene"},{"created":"2022-03-22T10:54:32.145022+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11708","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: was has been classified as Green List (High Evidence).","entity_name":"WAS","entity_type":"gene"},{"created":"2022-03-22T10:54:22.432927+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11708","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WAS were changed from  to Wiskott-Aldrich syndrome, MIM# 301000; Thrombocytopaenia, X-linked, MIM# 313900; Neutropenia, severe congenital, X-linked , MIM#300299","entity_name":"WAS","entity_type":"gene"},{"created":"2022-03-22T10:54:03.192099+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11707","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WAS were set to ","entity_name":"WAS","entity_type":"gene"},{"created":"2022-03-22T10:53:36.566651+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11706","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WAS was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"WAS","entity_type":"gene"},{"created":"2022-03-22T10:53:17.226062+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11705","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WAS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Wiskott-Aldrich syndrome, MIM# 301000, Thrombocytopaenia, X-linked, MIM# 313900, Neutropenia, severe congenital, X-linked , MIM#300299; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"WAS","entity_type":"gene"},{"created":"2022-03-22T10:16:38.796155+11:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.109","user_name":"Belinda Chong","item_type":"entity","text":"reviewed gene: USH2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 12427073, 20507924, 17296898, 19881469, 18273898; Phenotypes: Retinitis pigmentosa 39, MIM#613809; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"USH2A","entity_type":"gene"},{"created":"2022-03-22T08:45:42.483365+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11705","user_name":"Abhijit Kulkarni","item_type":"entity","text":"reviewed gene: WAS: Rating: GREEN; Mode of pathogenicity: None; Publications: 30969660, 34307257, 20301357; Phenotypes: Congenital Neutropenia, Throbocytopenia, Immunodefeciency, Eczema; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"WAS","entity_type":"gene"},{"created":"2022-03-21T18:40:41.334793+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UNC13D as ready","entity_name":"UNC13D","entity_type":"gene"},{"created":"2022-03-21T18:40:41.320431+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: unc13d has been classified as Green List (High Evidence).","entity_name":"UNC13D","entity_type":"gene"},{"created":"2022-03-21T18:40:38.555000+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UNC13D were changed from  to Haemophagocytic lymphohistiocytosis, familial, 3 MIM#608898","entity_name":"UNC13D","entity_type":"gene"},{"created":"2022-03-21T18:40:12.220892+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UNC13D were set to ","entity_name":"UNC13D","entity_type":"gene"},{"created":"2022-03-21T18:39:40.866010+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UNC13D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"UNC13D","entity_type":"gene"},{"created":"2022-03-21T18:39:08.177376+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: UNC13D: Rating: GREEN; Mode of pathogenicity: None; Publications: 14622600, 16825436, 17993578; Phenotypes: Haemophagocytic lymphohistiocytosis, familial, 3 MIM#608898; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"UNC13D","entity_type":"gene"},{"created":"2022-03-21T18:38:52.807193+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11705","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UNC13D were changed from  to Haemophagocytic lymphohistiocytosis, familial, 3 MIM#608898","entity_name":"UNC13D","entity_type":"gene"},{"created":"2022-03-21T18:38:32.812536+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11704","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UNC13D were set to ","entity_name":"UNC13D","entity_type":"gene"},{"created":"2022-03-21T18:38:04.607615+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11703","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UNC13D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"UNC13D","entity_type":"gene"},{"created":"2022-03-21T18:32:57.978519+11:00","panel_name":"Complement Deficiencies","panel_id":224,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C8A as ready","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:32:57.968686+11:00","panel_name":"Complement Deficiencies","panel_id":224,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c8a has been classified as Amber List (Moderate Evidence).","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:32:54.850740+11:00","panel_name":"Complement Deficiencies","panel_id":224,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C8A were changed from  to C8 deficiency, type I MIM#613790","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:32:24.739447+11:00","panel_name":"Complement Deficiencies","panel_id":224,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: C8A were set to ","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:31:39.340011+11:00","panel_name":"Complement Deficiencies","panel_id":224,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C8A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:31:10.310433+11:00","panel_name":"Complement Deficiencies","panel_id":224,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: C8A as Amber List (moderate evidence)","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:31:10.299067+11:00","panel_name":"Complement Deficiencies","panel_id":224,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c8a has been classified as Amber List (Moderate Evidence).","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:30:39.506271+11:00","panel_name":"Complement Deficiencies","panel_id":224,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: C8A: Rating: AMBER; Mode of pathogenicity: None; Publications: 9759902, 32769119; Phenotypes: C8 deficiency, type I MIM#613790; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:29:33.279632+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11702","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C8A as ready","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:29:33.268405+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11702","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c8a has been classified as Amber List (Moderate Evidence).","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:29:25.303185+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11702","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C8A were changed from  to C8 deficiency, type I MIM#613790","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:29:04.818376+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11701","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: C8A were set to ","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:28:45.297376+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11700","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C8A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:28:26.234179+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11699","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: C8A as Amber List (moderate evidence)","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:28:26.223261+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11699","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c8a has been classified as Amber List (Moderate Evidence).","entity_name":"C8A","entity_type":"gene"},{"created":"2022-03-21T18:27:47.721313+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11698","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SAMHD1 as ready","entity_name":"SAMHD1","entity_type":"gene"},{"created":"2022-03-21T18:27:47.709993+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11698","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: samhd1 has been classified as Green List (High Evidence).","entity_name":"SAMHD1","entity_type":"gene"},{"created":"2022-03-21T18:27:37.861257+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11698","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SAMHD1 were changed from  to Aicardi-Goutieres syndrome 5, MIM# 612952","entity_name":"SAMHD1","entity_type":"gene"},{"created":"2022-03-21T18:27:15.917701+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11697","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SAMHD1 were set to ","entity_name":"SAMHD1","entity_type":"gene"},{"created":"2022-03-21T18:26:55.399693+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11696","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SAMHD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SAMHD1","entity_type":"gene"},{"created":"2022-03-21T18:25:56.176870+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11695","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UNC119 as ready","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:25:56.165710+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11695","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: unc119 has been classified as Green List (High Evidence).","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:25:48.555362+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11695","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UNC119 were changed from  to Cone-rod dystrophy, MONDO:0015993; Immunodeficiency 13 MIM#615518","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:25:28.981454+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11694","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UNC119 were set to ","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:25:02.760238+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11693","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UNC119 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:24:41.105174+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11692","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UNC119 as Green List (high evidence)","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:24:41.095417+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11692","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: unc119 has been classified as Green List (High Evidence).","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:24:12.124894+11:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UNC119 as ready","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:24:12.113921+11:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: unc119 has been classified as Green List (High Evidence).","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:24:07.774029+11:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UNC119 were set to 30679166","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:23:55.157038+11:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UNC119 were changed from ?Cone-rod dystrophy to Cone-rod dystrophy, MONDO:0015993","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:23:37.156373+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11691","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Immunodeficiency 13: Single case reported with the missense Gly22Val. The allele frequency of this variant is >2% in the African/African American subpopulation in gnomAD v2.1, including 6 homozygotes. RED for this association.\r\n\r\nAmber for association with cone-rod dystrophy.; to: Immunodeficiency 13: Single case reported with the missense Gly22Val. The allele frequency of this variant is >2% in the African/African American subpopulation in gnomAD v2.1, including 6 homozygotes. RED for this association.\r\n\r\nBorderline Green for association with cone-rod dystrophy.","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:23:24.940960+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11691","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: UNC119: Changed rating: GREEN","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:23:06.446897+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11691","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UNC119 as Amber List (moderate evidence)","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:23:06.434411+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11691","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: unc119 has been classified as Amber List (Moderate Evidence).","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:22:48.030454+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11690","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: UNC119: Rating: AMBER; Mode of pathogenicity: None; Publications: 22184408; Phenotypes: Cone-rod dystrophy, MONDO:0015993, Immunodeficiency 13 MIM#615518; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UNC119","entity_type":"gene"},{"created":"2022-03-21T18:19:57.030056+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11690","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SAMD9 as ready","entity_name":"SAMD9","entity_type":"gene"},{"created":"2022-03-21T18:19:57.018322+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11690","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: samd9 has been classified as Green List (High Evidence).","entity_name":"SAMD9","entity_type":"gene"},{"created":"2022-03-21T18:18:18.831191+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11690","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SAMD9 were changed from  to MIRAGE syndrome, MIM#617053; Tumoral calcinosis, familial, normophosphatemic, MIM#610455; Monosomy 7 myelodysplasia and leukemia syndrome 2, MIM# 619041","entity_name":"SAMD9","entity_type":"gene"},{"created":"2022-03-21T18:17:59.268802+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11689","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SAMD9 were set to ","entity_name":"SAMD9","entity_type":"gene"},{"created":"2022-03-21T18:17:04.170839+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11688","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SAMD9 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"SAMD9","entity_type":"gene"},{"created":"2022-03-21T18:16:44.620187+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11687","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SAMD9: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: MIRAGE syndrome, MIM#617053, Tumoral calcinosis, familial, normophosphatemic, MIM#610455, Monosomy 7 myelodysplasia and leukemia syndrome 2, MIM# 619041; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"SAMD9","entity_type":"gene"},{"created":"2022-03-21T18:11:11.174781+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11687","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UCP3 as ready","entity_name":"UCP3","entity_type":"gene"},{"created":"2022-03-21T18:11:11.165322+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11687","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ucp3 has been classified as Red List (Low Evidence).","entity_name":"UCP3","entity_type":"gene"},{"created":"2022-03-21T18:11:01.335387+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11687","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UCP3 were set to ","entity_name":"UCP3","entity_type":"gene"},{"created":"2022-03-21T18:10:38.096779+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11686","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UCP3 were changed from  to {Obesity, severe, and type II diabetes}, MIM#601665","entity_name":"UCP3","entity_type":"gene"},{"created":"2022-03-21T18:10:11.906515+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11685","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UCP3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UCP3","entity_type":"gene"},{"created":"2022-03-21T18:09:53.061340+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11684","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UCP3 as Red List (low evidence)","entity_name":"UCP3","entity_type":"gene"},{"created":"2022-03-21T18:09:53.052647+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11684","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ucp3 has been classified as Red List (Low Evidence).","entity_name":"UCP3","entity_type":"gene"},{"created":"2022-03-21T18:08:08.287325+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11683","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFS3 as ready","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:08:08.277855+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11683","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufs3 has been classified as Green List (High Evidence).","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:08:00.505038+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11683","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFS3 were changed from  to Mitochondrial complex I deficiency, nuclear type 8 - MIM#618230","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:07:41.080773+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11682","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFS3 were set to ","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:07:18.772386+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11681","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFS3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:06:44.413818+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.402","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFS3 as ready","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:06:44.402124+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.402","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufs3 has been classified as Red List (Low Evidence).","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:03:15.520550+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.402","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFS3 were changed from  to Mitochondrial complex I deficiency, nuclear type 8 - MIM#618230","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:02:32.821227+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.401","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFS3 were set to ","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:01:58.190378+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.400","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFS3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:01:29.219945+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.399","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFS3 as Red List (low evidence)","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:01:29.210810+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.399","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufs3 has been classified as Red List (Low Evidence).","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:00:28.997646+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.743","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFS3 as ready","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:00:28.986366+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.743","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufs3 has been classified as Green List (High Evidence).","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T18:00:22.399246+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.743","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFS3 were changed from  to Mitochondrial complex I deficiency, nuclear type 8 - MIM#618230","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T17:59:44.131834+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.742","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFS3 were set to ","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T17:59:04.792369+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.741","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFS3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T17:58:03.919400+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.442","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFS3 as ready","entity_name":"NDUFS3","entity_type":"gene"},{"created":"2022-03-21T17:58:03.899510+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.442","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufs3 has been classified as Green List (High Evidence).","entity_name":"NDUFS3","entity_type":"gene"}]}