{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=929","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=927","results":[{"created":"2022-03-19T13:04:07.180174+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11588","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VKORC1 were changed from  to Vitamin K-dependent clotting factors, combined deficiency of, 2, MIM# 607473; Warfarin resistance, MIM# 122700","entity_name":"VKORC1","entity_type":"gene"},{"created":"2022-03-19T13:03:47.322594+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11587","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VKORC1 were set to ","entity_name":"VKORC1","entity_type":"gene"},{"created":"2022-03-19T13:01:14.798512+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.332","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VIPAS39 as ready","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T13:01:14.784248+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.332","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vipas39 has been classified as Green List (High Evidence).","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T13:01:05.598811+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.332","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VIPAS39 were changed from Arthrogryposis, renal dysfunction, and cholestasis 2, MIM#613404 to Arthrogryposis, renal dysfunction, and cholestasis 2, MIM#613404","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T13:00:38.033596+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.331","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VIPAS39 were changed from  to Arthrogryposis, renal dysfunction, and cholestasis 2, MIM#613404","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T12:59:56.563963+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.330","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VIPAS39 were set to ","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T12:59:27.249054+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.329","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VIPAS39 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T12:58:43.706738+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.328","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VIPAS39: Rating: GREEN; Mode of pathogenicity: None; Publications: 20190753, 35151346; Phenotypes: Arthrogryposis, renal dysfunction, and cholestasis 2, MIM#613404; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T12:57:13.007767+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11586","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VIPAS39 as ready","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T12:57:12.996454+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11586","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vipas39 has been classified as Green List (High Evidence).","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T12:56:57.019173+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11586","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VIPAS39 were changed from  to Arthrogryposis, renal dysfunction, and cholestasis 2, MIM#613404","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T12:56:35.744043+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11585","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VIPAS39 were set to ","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T12:56:14.014061+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11584","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VIPAS39 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T12:55:36.702369+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11583","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VIPAS39: Rating: GREEN; Mode of pathogenicity: None; Publications: 20190753, 35151346; Phenotypes: Arthrogryposis, renal dysfunction, and cholestasis 2, MIM#613404; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VIPAS39","entity_type":"gene"},{"created":"2022-03-19T12:52:59.355707+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11583","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VEGFA as ready","entity_name":"VEGFA","entity_type":"gene"},{"created":"2022-03-19T12:52:59.345535+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11583","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vegfa has been classified as Red List (Low Evidence).","entity_name":"VEGFA","entity_type":"gene"},{"created":"2022-03-19T12:52:47.066748+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11583","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VEGFA were changed from  to {Microvascular complications of diabetes 1} 603933","entity_name":"VEGFA","entity_type":"gene"},{"created":"2022-03-19T12:52:25.424511+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11582","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VEGFA as Red List (low evidence)","entity_name":"VEGFA","entity_type":"gene"},{"created":"2022-03-19T12:52:25.410472+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11582","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vegfa has been classified as Red List (Low Evidence).","entity_name":"VEGFA","entity_type":"gene"},{"created":"2022-03-19T12:52:07.634255+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11581","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VEGFA: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Microvascular complications of diabetes 1} 603933; Mode of inheritance: None","entity_name":"VEGFA","entity_type":"gene"},{"created":"2022-03-19T12:50:52.077108+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11581","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VDR as ready","entity_name":"VDR","entity_type":"gene"},{"created":"2022-03-19T12:50:52.064811+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11581","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vdr has been classified as Green List (High Evidence).","entity_name":"VDR","entity_type":"gene"},{"created":"2022-03-19T12:50:40.525750+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11581","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VDR were changed from  to Rickets, vitamin D-resistant, type IIA, MIM# 277440","entity_name":"VDR","entity_type":"gene"},{"created":"2022-03-19T12:50:17.253515+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11580","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VDR were set to ","entity_name":"VDR","entity_type":"gene"},{"created":"2022-03-19T12:49:58.277363+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11579","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VDR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VDR","entity_type":"gene"},{"created":"2022-03-19T12:49:38.718671+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11578","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VDR: Rating: GREEN; Mode of pathogenicity: None; Publications: 2849209, 9005998, 17970811; Phenotypes: Rickets, vitamin D-resistant, type IIA, MIM# 277440; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VDR","entity_type":"gene"},{"created":"2022-03-19T12:46:43.049671+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11578","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VCL as ready","entity_name":"VCL","entity_type":"gene"},{"created":"2022-03-19T12:46:43.038257+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11578","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vcl has been classified as Green List (High Evidence).","entity_name":"VCL","entity_type":"gene"},{"created":"2022-03-19T12:46:35.353281+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11578","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VCL were changed from  to Cardiomyopathy, dilated, 1W, MIM# 611407","entity_name":"VCL","entity_type":"gene"},{"created":"2022-03-19T12:46:16.060415+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11577","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VCL were set to ","entity_name":"VCL","entity_type":"gene"},{"created":"2022-03-19T12:45:10.544946+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11576","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VCL was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VCL","entity_type":"gene"},{"created":"2022-03-19T12:44:53.323509+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11575","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VCL: Rating: GREEN; Mode of pathogenicity: None; Publications: 31983221, 32516855, 26406308, 26458567, 24062880, 11815424, 17785437, 17097056; Phenotypes: Cardiomyopathy, dilated, 1W, MIM# 611407; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VCL","entity_type":"gene"},{"created":"2022-03-19T12:42:26.890384+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11575","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VANGL2 as ready","entity_name":"VANGL2","entity_type":"gene"},{"created":"2022-03-19T12:42:26.877509+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11575","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vangl2 has been classified as Red List (Low Evidence).","entity_name":"VANGL2","entity_type":"gene"},{"created":"2022-03-19T12:42:14.317746+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11575","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VANGL2 were changed from  to Neural tube defects, MIM# 182940","entity_name":"VANGL2","entity_type":"gene"},{"created":"2022-03-19T12:41:54.760954+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11574","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VANGL2 were set to ","entity_name":"VANGL2","entity_type":"gene"},{"created":"2022-03-19T12:41:29.602848+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11573","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VANGL2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VANGL2","entity_type":"gene"},{"created":"2022-03-19T12:41:10.199079+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11572","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VANGL2 as Red List (low evidence)","entity_name":"VANGL2","entity_type":"gene"},{"created":"2022-03-19T12:41:10.188036+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11572","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vangl2 has been classified as Red List (Low Evidence).","entity_name":"VANGL2","entity_type":"gene"},{"created":"2022-03-19T12:40:52.562992+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11571","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VANGL2: Rating: RED; Mode of pathogenicity: None; Publications: 20558380, 20738329, 34842271; Phenotypes: Neural tube defects, MIM# 182940; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VANGL2","entity_type":"gene"},{"created":"2022-03-19T12:35:10.387921+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11571","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VANGL1 as ready","entity_name":"VANGL1","entity_type":"gene"},{"created":"2022-03-19T12:35:10.378269+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11571","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vangl1 has been classified as Red List (Low Evidence).","entity_name":"VANGL1","entity_type":"gene"},{"created":"2022-03-19T12:34:58.845860+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11571","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VANGL1 were changed from  to Caudal regression syndrome, MIM# 600145; {Neural tube defects, susceptibility to} 182940","entity_name":"VANGL1","entity_type":"gene"},{"created":"2022-03-19T12:34:37.206310+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11570","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VANGL1 were set to ","entity_name":"VANGL1","entity_type":"gene"},{"created":"2022-03-19T12:34:17.678996+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11569","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VANGL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VANGL1","entity_type":"gene"},{"created":"2022-03-19T12:33:59.533927+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11568","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VANGL1 as Red List (low evidence)","entity_name":"VANGL1","entity_type":"gene"},{"created":"2022-03-19T12:33:59.521568+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11568","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vangl1 has been classified as Red List (Low Evidence).","entity_name":"VANGL1","entity_type":"gene"},{"created":"2022-03-19T12:33:40.263828+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11567","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VANGL1: Rating: RED; Mode of pathogenicity: None; Publications: 17409324; Phenotypes: Caudal regression syndrome, MIM# 600145, {Neural tube defects, susceptibility to} 182940; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VANGL1","entity_type":"gene"},{"created":"2022-03-19T12:29:25.286977+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.433","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VAMP1 as ready","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:29:25.267246+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.433","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vamp1 has been classified as Red List (Low Evidence).","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:29:22.691872+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.433","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VAMP1 were changed from  to Spastic ataxia 1, autosomal dominant, MIM# 108600","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:28:53.852904+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.432","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VAMP1 were set to ","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:28:27.217993+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.431","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VAMP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:27:56.945331+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.430","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VAMP1 as Red List (low evidence)","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:27:56.935105+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.430","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vamp1 has been classified as Red List (Low Evidence).","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:27:28.372782+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.429","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VAMP1: Rating: RED; Mode of pathogenicity: None; Publications: 22958904; Phenotypes: Spastic ataxia 1, autosomal dominant, MIM# 108600; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:25:35.866345+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11567","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VAMP1 as ready","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:25:35.848597+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11567","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vamp1 has been classified as Green List (High Evidence).","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:25:28.389327+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11567","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VAMP1 were changed from  to Myasthenic syndrome, congenital, 25, MIM# 618323; Spastic ataxia 1, autosomal dominant, MIM# 108600","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:25:08.290848+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11566","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VAMP1 were set to ","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:24:48.629909+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11565","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VAMP1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:24:28.472965+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11564","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: VAMP1.","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T12:24:14.843875+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11564","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VAMP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28168212, 28253535, 28600779, 17102983, 22958904; Phenotypes: Myasthenic syndrome, congenital, 25, MIM# 618323, Spastic ataxia 1, autosomal dominant, MIM# 108600; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"VAMP1","entity_type":"gene"},{"created":"2022-03-19T11:47:16.094886+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11564","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFB8 as ready","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-19T11:47:16.075376+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11564","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufb8 has been classified as Green List (High Evidence).","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-19T11:47:07.427357+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11564","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFB8 were changed from  to Mitochondrial complex I deficiency, nuclear type 32 - MIM#618252","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-19T11:46:47.345663+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11563","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFB8 were set to ","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-19T11:46:24.741234+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11562","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFB8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-19T11:45:58.550100+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.733","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFB8 as ready","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-19T11:45:58.538420+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.733","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufb8 has been classified as Green List (High Evidence).","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-19T11:45:56.014946+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.733","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFB8 were changed from  to Mitochondrial complex I deficiency, nuclear type 32 - MIM#618252","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-19T11:45:18.327299+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.732","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFB8 were set to ","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-19T11:44:45.479692+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.731","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFB8 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-19T11:44:16.419554+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.731","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFB8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFB8","entity_type":"gene"},{"created":"2022-03-19T11:42:56.287902+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11561","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF7 as ready","entity_name":"NDUFAF7","entity_type":"gene"},{"created":"2022-03-19T11:42:56.278470+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11561","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf7 has been classified as Red List (Low Evidence).","entity_name":"NDUFAF7","entity_type":"gene"},{"created":"2022-03-19T11:42:43.149355+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11561","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF7 were changed from  to Pathologic myopia","entity_name":"NDUFAF7","entity_type":"gene"},{"created":"2022-03-19T11:42:23.801148+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11560","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF7 were set to ","entity_name":"NDUFAF7","entity_type":"gene"},{"created":"2022-03-19T11:42:03.108655+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11559","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF7 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NDUFAF7","entity_type":"gene"},{"created":"2022-03-19T11:41:43.329059+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11558","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFAF7 as Red List (low evidence)","entity_name":"NDUFAF7","entity_type":"gene"},{"created":"2022-03-19T11:41:43.317950+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11558","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf7 has been classified as Red List (Low Evidence).","entity_name":"NDUFAF7","entity_type":"gene"},{"created":"2022-03-19T11:40:37.338460+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11557","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FRA10AC1 were changed from  to Neurodevelopmental disorder, MONDO:0700092, FRA10AC1-related","entity_name":"FRA10AC1","entity_type":"gene"},{"created":"2022-03-19T11:40:15.439737+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11556","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FRA10AC1 were set to 15203205","entity_name":"FRA10AC1","entity_type":"gene"},{"created":"2022-03-19T11:39:50.438133+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11555","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FRA10AC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FRA10AC1","entity_type":"gene"},{"created":"2022-03-19T11:38:37.296563+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF4 as ready","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:38:37.284018+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf4 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:38:33.496138+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF4 were set to ","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:38:23.928025+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFAF4 as Amber List (moderate evidence)","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:38:23.914350+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf4 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:38:14.430237+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFAF4: Rating: AMBER; Mode of pathogenicity: None; Publications: 32949790, 28853723, 18179882; Phenotypes: Mitochondrial complex I deficiency, nuclear type 15 - MIM#618237; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:36:17.697796+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.429","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF4 as ready","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:36:17.685024+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.429","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf4 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:36:14.914101+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.429","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF4 were changed from  to Mitochondrial complex I deficiency, nuclear type 15 - MIM#618237","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:35:35.707051+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.428","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF4 were set to ","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:35:06.067241+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.427","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:21:49.606661+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.426","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFAF4 as Amber List (moderate evidence)","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:21:49.596048+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.426","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf4 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:21:00.329423+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.391","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF4 as ready","entity_name":"NDUFAF4","entity_type":"gene"},{"created":"2022-03-19T11:21:00.318219+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.391","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf4 has been classified as Red List (Low Evidence).","entity_name":"NDUFAF4","entity_type":"gene"}]}