{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=841","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=839","results":[{"created":"2022-05-14T17:58:31.334554+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14286","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MUT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MUT","entity_type":"gene"},{"created":"2022-05-14T17:58:04.449334+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14285","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MUT: Rating: GREEN; Mode of pathogenicity: None; Publications: 1977311, 11528502, 12948746; Phenotypes: Methylmalonic aciduria, mut(0) type, MIM# 251000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MUT","entity_type":"gene"},{"created":"2022-05-14T17:55:41.961644+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14285","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MVK as ready","entity_name":"MVK","entity_type":"gene"},{"created":"2022-05-14T17:55:41.951669+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14285","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mvk has been classified as Green List (High Evidence).","entity_name":"MVK","entity_type":"gene"},{"created":"2022-05-14T17:55:32.924173+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14285","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MVK were changed from  to Mevalonic aciduria MIM# 610377","entity_name":"MVK","entity_type":"gene"},{"created":"2022-05-14T17:54:50.276772+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14284","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MVK were set to ","entity_name":"MVK","entity_type":"gene"},{"created":"2022-05-14T17:54:28.516864+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14283","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MVK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MVK","entity_type":"gene"},{"created":"2022-05-14T17:54:08.052037+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14282","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MVK: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Mevalonic aciduria MIM#610377; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MVK","entity_type":"gene"},{"created":"2022-05-14T17:53:03.022785+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14282","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MXI1 as ready","entity_name":"MXI1","entity_type":"gene"},{"created":"2022-05-14T17:53:03.000475+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14282","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mxi1 has been classified as Red List (Low Evidence).","entity_name":"MXI1","entity_type":"gene"},{"created":"2022-05-14T17:52:46.483514+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14282","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MXI1 as Red List (low evidence)","entity_name":"MXI1","entity_type":"gene"},{"created":"2022-05-14T17:52:46.469830+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14282","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mxi1 has been classified as Red List (Low Evidence).","entity_name":"MXI1","entity_type":"gene"},{"created":"2022-05-14T17:51:48.136379+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14281","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MXI1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"MXI1","entity_type":"gene"},{"created":"2022-05-14T17:50:57.015533+10:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYD88 as ready","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T17:50:57.004693+10:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myd88 has been classified as Green List (High Evidence).","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T17:50:53.684366+10:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYD88 were changed from  to Immunodeficiency 68, MIM# 612260","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T17:50:21.751747+10:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYD88 were set to ","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T17:49:51.306915+10:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYD88 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T17:49:20.577614+10:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYD88: Rating: GREEN; Mode of pathogenicity: None; Publications: 18669862, 20538326, 31301515; Phenotypes: Immunodeficiency 68, MIM# 612260; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T17:48:34.179929+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14281","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYD88 as ready","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T17:48:34.169624+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14281","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myd88 has been classified as Green List (High Evidence).","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T17:48:24.627807+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14281","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYD88 were changed from  to Immunodeficiency 68, MIM# 612260","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T17:48:03.889514+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14280","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYD88 were set to ","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T17:47:41.780815+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14279","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYD88 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T17:47:16.778282+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14278","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYD88: Rating: GREEN; Mode of pathogenicity: None; Publications: 18669862, 20538326, 31301515; Phenotypes: Immunodeficiency 68, MIM# 612260; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYD88","entity_type":"gene"},{"created":"2022-05-14T13:46:17.600941+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14278","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYH14 as ready","entity_name":"MYH14","entity_type":"gene"},{"created":"2022-05-14T13:46:17.587492+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14278","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myh14 has been classified as Green List (High Evidence).","entity_name":"MYH14","entity_type":"gene"},{"created":"2022-05-14T13:34:00.418985+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14278","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYH14 were changed from  to Deafness, autosomal dominant 4A, MIM# 600652; Peripheral neuropathy, myopathy, hoarseness, and hearing loss 614369","entity_name":"MYH14","entity_type":"gene"},{"created":"2022-05-14T13:33:36.442408+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14277","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYH14 were set to ","entity_name":"MYH14","entity_type":"gene"},{"created":"2022-05-14T13:33:16.595009+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14276","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYH14 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYH14","entity_type":"gene"},{"created":"2022-05-14T13:32:56.235651+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14275","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYH14: Rating: GREEN; Mode of pathogenicity: None; Publications: 15015131, 25719458, 31045651, 28221712, 34681017, 21480433, 31653586, 31631044, 31231018; Phenotypes: Deafness, autosomal dominant 4A, MIM# 600652, Peripheral neuropathy, myopathy, hoarseness, and hearing loss  614369; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYH14","entity_type":"gene"},{"created":"2022-05-14T13:22:17.566194+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14275","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYH3 as ready","entity_name":"MYH3","entity_type":"gene"},{"created":"2022-05-14T13:22:17.552517+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14275","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myh3 has been classified as Green List (High Evidence).","entity_name":"MYH3","entity_type":"gene"},{"created":"2022-05-14T13:22:05.737227+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14275","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYH3 were changed from  to Arthrogryposis, distal, type 2A (Freeman-Sheldon) 193700; Arthrogryposis, distal, type 2B3 (Sheldon-Hall) 618436; Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A 178110; Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B 618469","entity_name":"MYH3","entity_type":"gene"},{"created":"2022-05-14T13:21:38.614398+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14274","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYH3 were set to ","entity_name":"MYH3","entity_type":"gene"},{"created":"2022-05-14T13:21:16.059091+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14273","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYH3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MYH3","entity_type":"gene"},{"created":"2022-05-14T13:20:55.352196+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14272","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYH3: Rating: GREEN; Mode of pathogenicity: None; Publications: 25957469, 26544689, 21531865, 18695058; Phenotypes: Arthrogryposis, distal, type 2A (Freeman-Sheldon) 193700, Arthrogryposis, distal, type 2B3 (Sheldon-Hall) 618436, Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A 178110, Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B 618469; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MYH3","entity_type":"gene"},{"created":"2022-05-14T13:19:02.423963+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14272","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO1E as ready","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:19:02.406253+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14272","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo1e has been classified as Green List (High Evidence).","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:18:57.621111+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.200","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO1E as ready","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:18:57.610306+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.200","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo1e has been classified as Green List (High Evidence).","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:18:45.240888+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.200","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYO1E were changed from  to Glomerulosclerosis, focal segmental, 6, MIM# 614131","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:18:37.523446+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14272","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYO1E were changed from  to Glomerulosclerosis, focal segmental, 6, MIM# 614131","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:18:13.085347+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.199","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYO1E were set to ","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:17:40.010433+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.198","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYO1E was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:17:06.601274+10:00","panel_name":"Proteinuria","panel_id":144,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYO1E: Rating: GREEN; Mode of pathogenicity: None; Publications: 21756023, 31520189, 25739341, 23977349; Phenotypes: Glomerulosclerosis, focal segmental, 6, MIM# 614131; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:16:50.961632+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14271","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYO1E were set to ","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:16:29.926894+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14270","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYO1E was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:15:49.183583+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14269","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYO1E: Rating: GREEN; Mode of pathogenicity: None; Publications: 21756023, 31520189, 25739341, 23977349; Phenotypes: Glomerulosclerosis, focal segmental, 6, MIM# 614131; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYO1E","entity_type":"gene"},{"created":"2022-05-14T13:10:16.633530+10:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WNT1 as ready","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T13:10:16.623085+10:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wnt1 has been classified as Green List (High Evidence).","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T13:10:11.697241+10:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WNT1 were changed from  to Osteogenesis imperfecta, type XV, MIM# 615220","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T13:09:42.682536+10:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WNT1 were set to ","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T13:09:09.167850+10:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WNT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T13:08:09.507375+10:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WNT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23499309, 23499310, 23656646, 26671912; Phenotypes: Osteogenesis imperfecta, type XV, MIM# 615220; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T13:06:20.302420+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14269","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WNT1 as ready","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T13:06:20.293157+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14269","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wnt1 has been classified as Green List (High Evidence).","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T13:06:08.641642+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14269","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WNT1 were changed from  to Osteogenesis imperfecta, type XV, MIM# 615220","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T13:05:47.973880+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14268","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WNT1 were set to ","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T13:05:27.612624+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14267","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WNT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T13:05:04.861754+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14266","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WNT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23499309, 23499310, 23656646, 26671912; Phenotypes: Osteogenesis imperfecta, type XV, MIM# 615220; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-05-14T12:55:36.178649+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14266","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WNK4 as ready","entity_name":"WNK4","entity_type":"gene"},{"created":"2022-05-14T12:55:36.165719+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14266","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wnk4 has been classified as Green List (High Evidence).","entity_name":"WNK4","entity_type":"gene"},{"created":"2022-05-14T12:55:27.563344+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14266","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WNK4 were changed from  to Pseudohypoaldosteronism, type IIB, MIM# 614491","entity_name":"WNK4","entity_type":"gene"},{"created":"2022-05-14T12:55:00.307922+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14265","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WNK4 were set to ","entity_name":"WNK4","entity_type":"gene"},{"created":"2022-05-14T12:54:38.982322+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14264","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WNK4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WNK4","entity_type":"gene"},{"created":"2022-05-14T12:54:18.971383+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14263","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WNK4: Rating: GREEN; Mode of pathogenicity: None; Publications: 22266938, 31044551; Phenotypes: Pseudohypoaldosteronism, type IIB, MIM# 614491; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WNK4","entity_type":"gene"},{"created":"2022-05-14T12:52:42.635483+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14263","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WNK1 as ready","entity_name":"WNK1","entity_type":"gene"},{"created":"2022-05-14T12:52:42.625930+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14263","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wnk1 has been classified as Green List (High Evidence).","entity_name":"WNK1","entity_type":"gene"},{"created":"2022-05-14T12:52:33.836726+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14263","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WNK1 were changed from  to Neuropathy, hereditary sensory and autonomic, type II, MIM# 201300; MONDO:0024309; Pseudohypoaldosteronism, type IIC, MIM# 614492","entity_name":"WNK1","entity_type":"gene"},{"created":"2022-05-14T12:52:12.345363+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14262","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WNK1 were set to ","entity_name":"WNK1","entity_type":"gene"},{"created":"2022-05-14T12:51:48.358683+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14261","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WNK1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"WNK1","entity_type":"gene"},{"created":"2022-05-14T12:51:04.998740+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14260","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association.\r\n\r\nNote mono-allelic variants are associated with pseudohypoaldosteronism; to: Well established gene-disease associations.\r\n","entity_name":"WNK1","entity_type":"gene"},{"created":"2022-05-14T12:44:32.971139+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14260","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: WNK1: Changed phenotypes: Neuropathy, hereditary sensory and autonomic, type II, MIM# 201300, MONDO:0024309, Pseudohypoaldosteronism, type IIC, MIM# 614492; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"WNK1","entity_type":"gene"},{"created":"2022-05-14T12:42:24.398585+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14260","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR4 as ready","entity_name":"WDR4","entity_type":"gene"},{"created":"2022-05-14T12:42:24.375033+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14260","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr4 has been classified as Green List (High Evidence).","entity_name":"WDR4","entity_type":"gene"},{"created":"2022-05-14T12:42:13.897733+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14260","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR4 were changed from  to Galloway-Mowat syndrome 6, OMIM #618347; Microcephaly, growth deficiency, seizures, and brain malformations, OMIM #618346","entity_name":"WDR4","entity_type":"gene"},{"created":"2022-05-14T12:36:13.201254+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14259","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR4 were set to ","entity_name":"WDR4","entity_type":"gene"},{"created":"2022-05-14T12:35:52.901269+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14258","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR4","entity_type":"gene"},{"created":"2022-05-14T12:35:25.171934+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14257","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR4: Rating: GREEN; Mode of pathogenicity: None; Publications: 26416026, 30079490, 29597095, 28617965; Phenotypes: Galloway-Mowat syndrome 6, OMIM #618347, Microcephaly, growth deficiency, seizures, and brain malformations, OMIM #618346; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR4","entity_type":"gene"},{"created":"2022-05-14T12:32:33.601331+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14257","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: WDR36 as Amber List (moderate evidence)","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:32:33.590029+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14257","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr36 has been classified as Amber List (Moderate Evidence).","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:32:10.619586+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14256","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Multiple individuals reported.\r\n\r\nHowever, note one of the earliest reported variants p.Asp658Gly is present in >1,000 individuals in gnomad, and another, p.Ala449Thr is present in >2000.; to: Multiple individuals reported. Adult-onset.\r\n\r\nHowever, note one of the earliest reported variants p.Asp658Gly is present in >1,000 individuals in gnomad, and another, p.Ala449Thr is present in >2000.","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:31:59.362816+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14256","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: WDR36: Changed rating: AMBER","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:31:00.644437+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14256","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: WDR36: Changed publications: 15677485, 18172102, 20813748, 34681019, 29540704","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:28:23.952286+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14256","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Multiple individuals reported.\r\n\r\nHowever, note one of the earliest reported variants p.Asp658Gly is present in >1,000 individuals in gnomad.; to: Multiple individuals reported.\r\n\r\nHowever, note one of the earliest reported variants p.Asp658Gly is present in >1,000 individuals in gnomad, and another, p.Ala449Thr is present in >2000.","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:26:32.739591+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14256","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR36 as ready","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:26:32.728351+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14256","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr36 has been classified as Green List (High Evidence).","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:26:24.390820+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14256","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR36 were changed from  to Glaucoma 1, open angle, G, MIM# 609887","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:26:04.048540+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14255","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR36 were set to ","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:25:44.115099+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14254","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR36 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:25:23.022838+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14253","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR36: Rating: GREEN; Mode of pathogenicity: None; Publications: 15677485, 18172102, 20813748; Phenotypes: Glaucoma 1, open angle, G, MIM# 609887; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WDR36","entity_type":"gene"},{"created":"2022-05-14T12:21:27.703668+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14253","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WASHC5 as ready","entity_name":"WASHC5","entity_type":"gene"},{"created":"2022-05-14T12:21:27.692401+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14253","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: washc5 has been classified as Green List (High Evidence).","entity_name":"WASHC5","entity_type":"gene"},{"created":"2022-05-14T12:21:19.402983+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14253","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WASHC5 were changed from  to Ritscher-Schinzel syndrome 1, MIM# 220210; Spastic paraplegia 8, autosomal dominant, MIM# 603563","entity_name":"WASHC5","entity_type":"gene"},{"created":"2022-05-14T12:20:50.865641+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14252","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WASHC5 were set to ","entity_name":"WASHC5","entity_type":"gene"},{"created":"2022-05-14T12:20:25.472610+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14251","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WASHC5 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"WASHC5","entity_type":"gene"},{"created":"2022-05-14T12:19:54.998917+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14250","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WASHC5: Rating: GREEN; Mode of pathogenicity: None; Publications: 17160902, 23455931, 30778698, 24065355, 33456446; Phenotypes: Ritscher-Schinzel syndrome 1, MIM# 220210, Spastic paraplegia 8, autosomal dominant, MIM# 603563; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"WASHC5","entity_type":"gene"},{"created":"2022-05-13T19:11:26.048973+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4770","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WASF1 were changed from  to Neurodevelopmental disorder with absent language and variable seizures , MIM#618707","entity_name":"WASF1","entity_type":"gene"},{"created":"2022-05-13T19:10:52.531457+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4769","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WASF1 were set to PMID: 29961568","entity_name":"WASF1","entity_type":"gene"}]}