{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=828","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=826","results":[{"created":"2022-05-20T15:28:40.465603+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14728","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FXR1 as ready","entity_name":"FXR1","entity_type":"gene"},{"created":"2022-05-20T15:28:40.453730+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14728","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fxr1 has been classified as Green List (High Evidence).","entity_name":"FXR1","entity_type":"gene"},{"created":"2022-05-20T15:14:49.939231+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14728","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: ETV2 as ready","entity_name":"ETV2","entity_type":"gene"},{"created":"2022-05-20T15:14:49.927196+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14728","user_name":"Ain Roesley","item_type":"entity","text":"Gene: etv2 has been classified as Red List (Low Evidence).","entity_name":"ETV2","entity_type":"gene"},{"created":"2022-05-20T15:14:28.723206+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14728","user_name":"Ain Roesley","item_type":"entity","text":"gene: ETV2 was added\ngene: ETV2 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: ETV2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ETV2 were set to 33359164\nPhenotypes for gene: ETV2 were set to multiple fetal anomalies; congenital heart disease MONDO:000545, ETV2-related; vertebral malformations\nReview for gene: ETV2 was set to RED\ngene: ETV2 was marked as current diagnostic\nAdded comment: 1 family with 4 fetus-es, cHet for a fs (NMD-predicted) and a missense\r\n\r\n3/4 vertebral malformations\r\n2/4 Tetralogy of Fallot\r\n1/4 arterial septal defect\r\n1/4 ventricular septal defect, aortic dilatation\r\n1/4 pre-axial polydactyly \nSources: Literature","entity_name":"ETV2","entity_type":"gene"},{"created":"2022-05-20T15:00:03.363429+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14727","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GABRB2 as ready","entity_name":"GABRB2","entity_type":"gene"},{"created":"2022-05-20T15:00:03.315134+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14727","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gabrb2 has been classified as Green List (High Evidence).","entity_name":"GABRB2","entity_type":"gene"},{"created":"2022-05-20T14:37:17.531269+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14727","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GABRB2 were set to ","entity_name":"GABRB2","entity_type":"gene"},{"created":"2022-05-20T14:35:58.897738+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14726","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GALNT2 as ready","entity_name":"GALNT2","entity_type":"gene"},{"created":"2022-05-20T14:35:58.884689+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14726","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: galnt2 has been classified as Green List (High Evidence).","entity_name":"GALNT2","entity_type":"gene"},{"created":"2022-05-20T14:35:47.944969+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14726","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GALNT2 were changed from Congenital disorder of glycosylation to Congenital disorder of glycosylation MONDO:0015286","entity_name":"GALNT2","entity_type":"gene"},{"created":"2022-05-20T14:34:40.267424+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14725","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GALNT3 as ready","entity_name":"GALNT3","entity_type":"gene"},{"created":"2022-05-20T14:34:40.253530+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14725","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: galnt3 has been classified as Green List (High Evidence).","entity_name":"GALNT3","entity_type":"gene"},{"created":"2022-05-20T14:34:23.720581+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14725","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GALNT3 were changed from  to Tumoral calcinosis, hyperphosphatemic, familial, 1, MIM# 211900","entity_name":"GALNT3","entity_type":"gene"},{"created":"2022-05-20T14:34:00.724963+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14724","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GALNT3 were set to ","entity_name":"GALNT3","entity_type":"gene"},{"created":"2022-05-20T14:33:31.220234+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14723","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GALNT3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GALNT3","entity_type":"gene"},{"created":"2022-05-20T14:32:26.865487+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14722","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GALT as ready","entity_name":"GALT","entity_type":"gene"},{"created":"2022-05-20T14:32:26.853377+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14722","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: galt has been classified as Green List (High Evidence).","entity_name":"GALT","entity_type":"gene"},{"created":"2022-05-20T14:31:58.834645+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14722","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GALT were changed from  to Galactosaemia MIM#230400; Disorders of galactose metabolism","entity_name":"GALT","entity_type":"gene"},{"created":"2022-05-20T14:31:30.123735+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14721","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GALT were set to ","entity_name":"GALT","entity_type":"gene"},{"created":"2022-05-20T14:31:07.641254+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14720","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GALT was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GALT","entity_type":"gene"},{"created":"2022-05-20T14:30:08.843074+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14719","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GAMT as ready","entity_name":"GAMT","entity_type":"gene"},{"created":"2022-05-20T14:30:08.830233+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14719","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gamt has been classified as Green List (High Evidence).","entity_name":"GAMT","entity_type":"gene"},{"created":"2022-05-20T14:30:00.679524+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14719","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GAMT were changed from  to Cerebral creatine deficiency syndrome 2 MIM#612736; Disorders of creatinine metabolism","entity_name":"GAMT","entity_type":"gene"},{"created":"2022-05-20T14:29:39.001587+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14718","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GAMT were set to ","entity_name":"GAMT","entity_type":"gene"},{"created":"2022-05-20T14:29:17.137994+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14717","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GAMT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GAMT","entity_type":"gene"},{"created":"2022-05-20T14:28:39.411010+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14716","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GAN as ready","entity_name":"GAN","entity_type":"gene"},{"created":"2022-05-20T14:28:39.398243+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14716","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gan has been classified as Green List (High Evidence).","entity_name":"GAN","entity_type":"gene"},{"created":"2022-05-20T14:28:30.769600+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14716","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GAN were changed from  to Giant axonal neuropathy-1, MIM# 256850","entity_name":"GAN","entity_type":"gene"},{"created":"2022-05-20T14:28:03.817600+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14715","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GAN were set to ","entity_name":"GAN","entity_type":"gene"},{"created":"2022-05-20T14:27:43.118772+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14714","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GAN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GAN","entity_type":"gene"},{"created":"2022-05-20T14:26:25.266063+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14713","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GBA2 as ready","entity_name":"GBA2","entity_type":"gene"},{"created":"2022-05-20T14:26:25.251236+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14713","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gba2 has been classified as Green List (High Evidence).","entity_name":"GBA2","entity_type":"gene"},{"created":"2022-05-20T14:26:15.921614+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14713","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GBA2 were changed from  to Spastic paraplegia 46, autosomal recessive, MIM# 614409; MONDO:0013737","entity_name":"GBA2","entity_type":"gene"},{"created":"2022-05-20T14:25:53.443583+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14712","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GBA2 were set to ","entity_name":"GBA2","entity_type":"gene"},{"created":"2022-05-20T14:25:23.180413+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14711","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GBA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GBA2","entity_type":"gene"},{"created":"2022-05-20T14:24:37.057442+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14710","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GCDH as ready","entity_name":"GCDH","entity_type":"gene"},{"created":"2022-05-20T14:24:37.043369+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14710","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gcdh has been classified as Green List (High Evidence).","entity_name":"GCDH","entity_type":"gene"},{"created":"2022-05-20T14:24:28.445713+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14710","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GCDH were changed from  to Glutaric aciduria, type I MIM#231670; Organic acidurias","entity_name":"GCDH","entity_type":"gene"},{"created":"2022-05-20T14:24:02.015312+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14709","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GCDH were set to ","entity_name":"GCDH","entity_type":"gene"},{"created":"2022-05-20T14:23:39.258258+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14708","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GCDH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GCDH","entity_type":"gene"},{"created":"2022-05-20T14:22:49.001198+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14707","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GCH1 as ready","entity_name":"GCH1","entity_type":"gene"},{"created":"2022-05-20T14:22:48.989644+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14707","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gch1 has been classified as Green List (High Evidence).","entity_name":"GCH1","entity_type":"gene"},{"created":"2022-05-20T14:18:59.239237+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14707","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GCH1 were changed from  to Hyperphenylalaninemia, BH4-deficient, B, MIM# 233910; Dystonia, DOPA-responsive, with or without hyperphenylalaninemia, MIM# 128230","entity_name":"GCH1","entity_type":"gene"},{"created":"2022-05-20T14:18:36.402336+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14706","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GCH1 were set to ","entity_name":"GCH1","entity_type":"gene"},{"created":"2022-05-20T14:17:46.283275+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14705","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GCH1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"GCH1","entity_type":"gene"},{"created":"2022-05-20T13:59:39.186526+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14704","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GCK as ready","entity_name":"GCK","entity_type":"gene"},{"created":"2022-05-20T13:59:39.171052+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14704","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gck has been classified as Green List (High Evidence).","entity_name":"GCK","entity_type":"gene"},{"created":"2022-05-20T13:59:29.916184+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14704","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GCK were changed from  to Diabetes mellitus, noninsulin-dependent, late onset, AD (MIM#125853); Diabetes mellitus, permanent neonatal 1, AR (MIM#606176); Hyperinsulinemic hypoglycemia, familial, 3, AD (MIM#602485); MODY, type II, AD (MIM#125851)","entity_name":"GCK","entity_type":"gene"},{"created":"2022-05-20T13:59:09.222070+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14703","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GCK were set to ","entity_name":"GCK","entity_type":"gene"},{"created":"2022-05-20T13:58:46.527560+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14702","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GCK was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"GCK","entity_type":"gene"},{"created":"2022-05-20T13:58:03.025861+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14701","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GCNT2 as ready","entity_name":"GCNT2","entity_type":"gene"},{"created":"2022-05-20T13:58:03.009827+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14701","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gcnt2 has been classified as Green List (High Evidence).","entity_name":"GCNT2","entity_type":"gene"},{"created":"2022-05-20T13:57:55.632999+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14701","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: GDNF were changed from  to {Hirschsprung disease, susceptibility to, 3} MIM#613711","entity_name":"GDNF","entity_type":"gene"},{"created":"2022-05-20T13:57:54.236991+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14700","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GCNT2 were changed from  to Cataract 13 with adult i phenotype, OMIM # 116700","entity_name":"GCNT2","entity_type":"gene"},{"created":"2022-05-20T13:57:46.255453+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14700","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: GDNF were set to ","entity_name":"GDNF","entity_type":"gene"},{"created":"2022-05-20T13:57:41.698597+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14700","user_name":"Elena Savva","item_type":"entity","text":"Mode of inheritance for gene: GDNF was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","entity_name":"GDNF","entity_type":"gene"},{"created":"2022-05-20T13:57:26.710766+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14699","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GCNT2 were set to ","entity_name":"GCNT2","entity_type":"gene"},{"created":"2022-05-20T13:56:55.855594+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14698","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GCNT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GCNT2","entity_type":"gene"},{"created":"2022-05-20T13:55:48.988575+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14697","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GDAP1 as ready","entity_name":"GDAP1","entity_type":"gene"},{"created":"2022-05-20T13:55:48.976458+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14697","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gdap1 has been classified as Green List (High Evidence).","entity_name":"GDAP1","entity_type":"gene"},{"created":"2022-05-20T13:55:40.042254+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14697","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GDAP1 were changed from  to Charcot-Marie-Tooth disease, axonal, type 2K 607831, MIM# Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, MIM# 607706; Charcot-Marie-Tooth disease, recessive intermediate, A, MIM# 608340; Charcot-Marie-Tooth disease, type 4A, MIM# 214400","entity_name":"GDAP1","entity_type":"gene"},{"created":"2022-05-20T13:54:42.483877+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14696","user_name":"Elena Savva","item_type":"entity","text":"Mode of inheritance for gene: ATPAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ATPAF2","entity_type":"gene"},{"created":"2022-05-20T13:53:55.337731+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14695","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: GATAD1 were changed from  to ?Cardiomyopathy, dilated, 2B MIM#614672","entity_name":"GATAD1","entity_type":"gene"},{"created":"2022-05-20T13:53:16.554324+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14694","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: GATAD1 as ready","entity_name":"GATAD1","entity_type":"gene"},{"created":"2022-05-20T13:53:16.536683+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14694","user_name":"Elena Savva","item_type":"entity","text":"Gene: gatad1 has been classified as Red List (Low Evidence).","entity_name":"GATAD1","entity_type":"gene"},{"created":"2022-05-20T13:42:30.478168+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14694","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: GATAD1 were set to ","entity_name":"GATAD1","entity_type":"gene"},{"created":"2022-05-20T13:42:24.939595+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14694","user_name":"Elena Savva","item_type":"entity","text":"Mode of inheritance for gene: GATAD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GATAD1","entity_type":"gene"},{"created":"2022-05-20T13:42:06.900519+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14693","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: FBXW4 as ready","entity_name":"FBXW4","entity_type":"gene"},{"created":"2022-05-20T13:42:06.888434+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14693","user_name":"Elena Savva","item_type":"entity","text":"Gene: fbxw4 has been classified as Red List (Low Evidence).","entity_name":"FBXW4","entity_type":"gene"},{"created":"2022-05-20T13:41:19.137777+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14693","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: AURKC were changed from  to Spermatogenic failure 5 MIM #243060","entity_name":"AURKC","entity_type":"gene"},{"created":"2022-05-20T13:41:13.209007+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14692","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: AURKC as ready","entity_name":"AURKC","entity_type":"gene"},{"created":"2022-05-20T13:41:13.187377+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14692","user_name":"Elena Savva","item_type":"entity","text":"Gene: aurkc has been classified as Red List (Low Evidence).","entity_name":"AURKC","entity_type":"gene"},{"created":"2022-05-20T13:41:06.856840+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14692","user_name":"Elena Savva","item_type":"entity","text":"Mode of inheritance for gene: AURKC was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"AURKC","entity_type":"gene"},{"created":"2022-05-20T13:40:54.178965+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14691","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ATPAF2 as ready","entity_name":"ATPAF2","entity_type":"gene"},{"created":"2022-05-20T13:40:54.166053+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14691","user_name":"Elena Savva","item_type":"entity","text":"Gene: atpaf2 has been classified as Red List (Low Evidence).","entity_name":"ATPAF2","entity_type":"gene"},{"created":"2022-05-20T13:40:46.048215+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14691","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ATP2C2 as ready","entity_name":"ATP2C2","entity_type":"gene"},{"created":"2022-05-20T13:40:46.034975+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14691","user_name":"Elena Savva","item_type":"entity","text":"Gene: atp2c2 has been classified as Red List (Low Evidence).","entity_name":"ATP2C2","entity_type":"gene"},{"created":"2022-05-20T13:40:37.254142+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14691","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: AHSG as ready","entity_name":"AHSG","entity_type":"gene"},{"created":"2022-05-20T13:40:37.233182+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14691","user_name":"Elena Savva","item_type":"entity","text":"Gene: ahsg has been classified as Red List (Low Evidence).","entity_name":"AHSG","entity_type":"gene"},{"created":"2022-05-20T13:40:23.605381+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14691","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GDAP1 were set to ","entity_name":"GDAP1","entity_type":"gene"},{"created":"2022-05-20T13:40:01.082619+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14690","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GDAP1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"GDAP1","entity_type":"gene"},{"created":"2022-05-20T13:38:57.584242+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14689","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GDF2 as ready","entity_name":"GDF2","entity_type":"gene"},{"created":"2022-05-20T13:38:57.571397+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14689","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gdf2 has been classified as Green List (High Evidence).","entity_name":"GDF2","entity_type":"gene"},{"created":"2022-05-20T13:38:47.324454+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14689","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GDF2 were changed from  to Telangiectasia, hereditary hemorrhagic, type 5 OMIM # 615506; pulmonary arteriovenous malformations","entity_name":"GDF2","entity_type":"gene"},{"created":"2022-05-20T13:38:24.941039+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14688","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GDF2 were set to ","entity_name":"GDF2","entity_type":"gene"},{"created":"2022-05-20T13:37:30.586011+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14687","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GDF2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"GDF2","entity_type":"gene"},{"created":"2022-05-20T13:36:44.397536+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14686","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GDF9 as ready","entity_name":"GDF9","entity_type":"gene"},{"created":"2022-05-20T13:36:44.374144+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14686","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gdf9 has been classified as Green List (High Evidence).","entity_name":"GDF9","entity_type":"gene"},{"created":"2022-05-20T13:36:34.836651+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14686","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GDF9 were changed from  to Premature ovarian failure 14, OMIM# 618014","entity_name":"GDF9","entity_type":"gene"},{"created":"2022-05-20T13:36:07.984298+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14685","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GDF9 were set to ","entity_name":"GDF9","entity_type":"gene"},{"created":"2022-05-20T13:34:05.135679+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14684","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GDF9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GDF9","entity_type":"gene"},{"created":"2022-05-20T13:33:18.051752+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14683","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GEMIN4 as ready","entity_name":"GEMIN4","entity_type":"gene"},{"created":"2022-05-20T13:33:18.032288+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14683","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gemin4 has been classified as Green List (High Evidence).","entity_name":"GEMIN4","entity_type":"gene"},{"created":"2022-05-20T13:33:09.027824+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14683","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GEMIN4 were changed from  to Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities, MIM# 617913","entity_name":"GEMIN4","entity_type":"gene"},{"created":"2022-05-20T13:32:47.297345+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14682","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GEMIN4 were set to ","entity_name":"GEMIN4","entity_type":"gene"},{"created":"2022-05-20T13:32:19.862950+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14681","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GEMIN4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GEMIN4","entity_type":"gene"},{"created":"2022-05-20T13:31:04.326936+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14680","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GFM2 as ready","entity_name":"GFM2","entity_type":"gene"},{"created":"2022-05-20T13:31:04.306703+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14680","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gfm2 has been classified as Green List (High Evidence).","entity_name":"GFM2","entity_type":"gene"},{"created":"2022-05-20T13:30:54.367974+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14680","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GFM2 were changed from  to Combined oxidative phosphorylation deficiency 39, OMIM #618397","entity_name":"GFM2","entity_type":"gene"}]}