{"count":221272,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1032","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1030","results":[{"created":"2022-01-24T08:50:28.390565+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.686","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UQCRC2 as Green List (high evidence)","entity_name":"UQCRC2","entity_type":"gene"},{"created":"2022-01-24T08:50:28.379909+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.686","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: uqcrc2 has been classified as Green List (High Evidence).","entity_name":"UQCRC2","entity_type":"gene"},{"created":"2022-01-23T13:10:32.451818+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10741","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNHD1 were changed from Male infertility due to sperm motility disorder (MONDO:0018395) to Spermatogenic failure 65, MIM# 619712","entity_name":"DNHD1","entity_type":"gene"},{"created":"2022-01-23T13:10:10.101982+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10740","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNHD1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Spermatogenic failure 65, MIM# 619712; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNHD1","entity_type":"gene"},{"created":"2022-01-23T11:25:38.295225+11:00","panel_name":"Growth failure","panel_id":3631,"panel_version":"1.30","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STT3A were changed from Congenital disorder of glycosylation, type Iw MIM#615596 to Congenital disorder of glycosylation, type Iw, AR, OMIM #615596; Congenital disorder of glycosylation, type Iw, autosomal dominant, MIM# 619714","entity_name":"STT3A","entity_type":"gene"},{"created":"2022-01-23T11:25:03.651862+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4458","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STT3A were changed from Congenital disorder of glycosylation, type Iw; OMIM #615596 to Congenital disorder of glycosylation, type Iw, AR, OMIM #615596; Congenital disorder of glycosylation, type Iw, autosomal dominant, MIM# 619714","entity_name":"STT3A","entity_type":"gene"},{"created":"2022-01-23T11:24:08.542225+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10740","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STT3A were changed from Congenital disorder of glycosylation, type Iw MIM#615596 to Congenital disorder of glycosylation, type Iw, AR, OMIM #615596; Congenital disorder of glycosylation, type Iw, autosomal dominant, MIM# 619714","entity_name":"STT3A","entity_type":"gene"},{"created":"2022-01-23T11:23:36.992400+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STT3A were changed from Congenital disorder of glycosylation, type Iw MIM#615596 to Congenital disorder of glycosylation, type Iw, AR, OMIM #615596; Congenital disorder of glycosylation, type Iw, autosomal dominant, MIM# 619714","entity_name":"STT3A","entity_type":"gene"},{"created":"2022-01-23T11:23:05.319403+11:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: STT3A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital disorder of glycosylation, type Iw, AR, OMIM #615596, Congenital disorder of glycosylation, type Iw, autosomal dominant, MIM# 619714; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"STT3A","entity_type":"gene"},{"created":"2022-01-23T11:22:46.615160+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"1.23","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STT3A were changed from Congenital disorder of glycosylation, type Iw; OMIM #615596 to Congenital disorder of glycosylation, type Iw, AR, OMIM #615596; Congenital disorder of glycosylation, type Iw, autosomal dominant, MIM# 619714","entity_name":"STT3A","entity_type":"gene"},{"created":"2022-01-23T11:22:07.310635+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"1.22","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: STT3A: Changed phenotypes: Congenital disorder of glycosylation, type Iw, AR, OMIM #615596, Congenital disorder of glycosylation, type Iw, autosomal dominant, MIM# 619714","entity_name":"STT3A","entity_type":"gene"},{"created":"2022-01-21T17:04:45.942376+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.66","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: CHD1 as Red List (low evidence)","entity_name":"CHD1","entity_type":"gene"},{"created":"2022-01-21T17:04:45.931771+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.66","user_name":"Chirag Patel","item_type":"entity","text":"Gene: chd1 has been classified as Red List (Low Evidence).","entity_name":"CHD1","entity_type":"gene"},{"created":"2022-01-21T17:04:39.296727+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.65","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: CHD1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"CHD1","entity_type":"gene"},{"created":"2022-01-21T12:52:48.717298+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2665","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their review","entity_name":"WNT1","entity_type":"gene"},{"created":"2022-01-21T12:50:54.871177+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2665","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: LD/ID reported in ~20% according to this cohort/literature review.; to: Robinow syndrome is characterized by dysmorphic features resembling a fetal face, mesomelic limb shortening, hypoplastic external genitalia in males, and renal and vertebral anomalies.","entity_name":"WNT5A","entity_type":"gene"},{"created":"2022-01-21T12:49:41.436153+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2665","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Although WNT7A-related conditions cause ulnar abnormalities, include in this panel due to phenotypic overlap (single forearm bone may be difficult to distinguish, particularly in non-specialist setting). \nSources: Expert list; to: Limb anomalies.\r\n\r\n\r\nSources: Expert list","entity_name":"WNT7A","entity_type":"gene"},{"created":"2022-01-21T12:47:22.603414+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2665","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their review","entity_name":"ZIC1","entity_type":"gene"},{"created":"2022-01-21T12:46:38.430598+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2665","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: 1 family (4 affected members), Weiss et al. (2017) identified a heterozygous nonsense ZNF462 mutation.\r\n3 additional unrelated patients with a similar phenotype with heterozygous ZNF462 mutations.\r\n14 unrelated patients with WSKA, Kruszka et al. (2019) identified heterozygous loss-of-function ZNF462 mutations.; to: 1 family (4 affected members), Weiss et al. (2017) identified a heterozygous nonsense ZNF462 mutation.\r\n3 additional unrelated patients with a similar phenotype with heterozygous ZNF462 mutations.\r\n14 unrelated patients with WSKA, Kruszka et al. (2019) identified heterozygous loss-of-function ZNF462 mutations.\r\n\r\nMultiple congenital anomalies syndrome.","entity_name":"ZNF462","entity_type":"gene"},{"created":"2022-01-21T12:41:31.392128+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2665","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXL2 as ready","entity_name":"FOXL2","entity_type":"gene"},{"created":"2022-01-21T12:41:31.378078+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2665","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxl2 has been classified as Red List (Low Evidence).","entity_name":"FOXL2","entity_type":"gene"},{"created":"2022-01-21T12:41:27.873166+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2665","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FOXL2 were changed from BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS SYNDROME to Blepharophimosis, epicanthus inversus, and ptosis, type 1 with premature ovarian insufficiency (POI) and type II without POI (MIM# 110100)","entity_name":"FOXL2","entity_type":"gene"},{"created":"2022-01-21T12:41:14.351690+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2664","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXL2 were set to ","entity_name":"FOXL2","entity_type":"gene"},{"created":"2022-01-21T12:41:00.410502+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2663","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FOXL2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FOXL2","entity_type":"gene"},{"created":"2022-01-21T12:38:18.902120+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2662","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FOXL2 as Red List (low evidence)","entity_name":"FOXL2","entity_type":"gene"},{"created":"2022-01-21T12:38:18.891912+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2662","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxl2 has been classified as Red List (Low Evidence).","entity_name":"FOXL2","entity_type":"gene"},{"created":"2022-01-21T12:30:12.123066+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2661","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FN1 as ready","entity_name":"FN1","entity_type":"gene"},{"created":"2022-01-21T12:30:12.111463+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2661","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fn1 has been classified as Amber List (Moderate Evidence).","entity_name":"FN1","entity_type":"gene"},{"created":"2022-01-21T12:29:52.466502+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2661","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FN1 were changed from Spondylometaphyseal Dysplasia with Corner Fractures to Spondylometaphyseal dysplasia, corner fracture type (MIM#184255)","entity_name":"FN1","entity_type":"gene"},{"created":"2022-01-21T12:29:39.563622+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2660","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FN1 were set to ","entity_name":"FN1","entity_type":"gene"},{"created":"2022-01-21T12:29:27.938051+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2659","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FN1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FN1","entity_type":"gene"},{"created":"2022-01-21T12:29:13.745477+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2658","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FN1: Rating: AMBER; Mode of pathogenicity: None; Publications: 33605604; Phenotypes: Spondylometaphyseal dysplasia, corner fracture type (MIM#184255); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FN1","entity_type":"gene"},{"created":"2022-01-21T12:26:55.808626+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4457","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FMN2 as ready","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T12:26:55.798256+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4457","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fmn2 has been classified as Green List (High Evidence).","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T12:26:51.976606+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4457","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FMN2 were changed from  to Intellectual developmental disorder, autosomal recessive 47, MIM#616193","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T12:26:16.578853+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4456","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FMN2 were set to ","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T12:22:52.371668+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4455","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FMN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T12:22:16.813002+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4454","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FMN2: Rating: GREEN; Mode of pathogenicity: None; Publications: 25480035, 32162566, 24161494; Phenotypes: Intellectual developmental disorder, autosomal recessive 47, MIM#616193; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T11:02:44.754492+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10739","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FMN2 as ready","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T11:02:44.739641+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10739","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fmn2 has been classified as Green List (High Evidence).","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T11:02:34.058646+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10739","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FMN2 were changed from  to Intellectual developmental disorder, autosomal recessive 47, MIM#616193","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T11:02:13.830370+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10738","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FMN2 were set to ","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T11:00:08.589424+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10737","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FMN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T10:59:43.774891+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10736","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FMN2: Rating: GREEN; Mode of pathogenicity: None; Publications: 25480035, 32162566, 24161494; Phenotypes: Intellectual developmental disorder, autosomal recessive 47, MIM#616193; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T10:55:49.735292+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2658","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FMN2 as ready","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T10:55:49.723689+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2658","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fmn2 has been classified as Red List (Low Evidence).","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T10:55:40.822045+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2658","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FMN2 were changed from NONSYNDROMIC AUTOSOMAL-RECESSIVE INTELLECTUAL DISABILITY to Intellectual developmental disorder, autosomal recessive 47, MIM#616193","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T10:55:24.503305+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2657","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FMN2 were set to ","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T10:55:10.275850+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2656","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FMN2 as Red List (low evidence)","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T10:55:10.263929+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2656","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fmn2 has been classified as Red List (Low Evidence).","entity_name":"FMN2","entity_type":"gene"},{"created":"2022-01-21T10:54:29.916074+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10736","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HAND1 as ready","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:54:29.905582+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10736","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hand1 has been classified as Amber List (Moderate Evidence).","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:54:18.759208+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10736","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HAND1 as Amber List (moderate evidence)","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:54:18.744892+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10736","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hand1 has been classified as Amber List (Moderate Evidence).","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:53:59.035823+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10735","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HAND1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:53:37.546709+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10734","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HAND1 were set to ","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:53:19.927432+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10733","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HAND1 were changed from  to Congenital heart disease, MONDO:0005453","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:52:55.974504+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.183","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HAND1 were changed from Congenital heart disease to Congenital heart disease, MONDO:0005453","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:52:12.227188+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2655","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HAND1 as ready","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:52:12.203100+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2655","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hand1 has been classified as Amber List (Moderate Evidence).","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:52:06.561403+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2655","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HAND1 were changed from Congenital heart defects to Congenital heart disease, MONDO:0005453","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:51:33.702224+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2654","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HAND1 were set to 19586923; 28112363; 18276607; 27942761; 31286141","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:51:18.788321+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2653","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HAND1 as Amber List (moderate evidence)","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:51:18.778095+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2653","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hand1 has been classified as Amber List (Moderate Evidence).","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:50:56.832725+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.182","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HAND1 as ready","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:50:56.820818+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.182","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hand1 has been classified as Amber List (Moderate Evidence).","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:50:54.409294+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.182","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HAND1 were changed from  to Congenital heart disease","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:50:29.128653+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.181","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HAND1 were set to ","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:49:59.562335+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.180","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HAND1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:49:36.742149+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.179","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HAND1 as Amber List (moderate evidence)","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:49:36.732739+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.179","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hand1 has been classified as Amber List (Moderate Evidence).","entity_name":"HAND1","entity_type":"gene"},{"created":"2022-01-21T10:47:47.513122+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2652","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FKBP8 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FKBP8","entity_type":"gene"},{"created":"2022-01-21T10:47:36.745154+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2651","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FKBP8 as Amber List (moderate evidence)","entity_name":"FKBP8","entity_type":"gene"},{"created":"2022-01-21T10:47:36.735936+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2651","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fkbp8 has been classified as Amber List (Moderate Evidence).","entity_name":"FKBP8","entity_type":"gene"},{"created":"2022-01-21T10:47:22.361054+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2650","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FKBP8: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Spina bifida, MONDO:0008449; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FKBP8","entity_type":"gene"},{"created":"2022-01-21T10:46:36.698316+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2650","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FKBP8 as ready","entity_name":"FKBP8","entity_type":"gene"},{"created":"2022-01-21T10:46:36.687474+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2650","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fkbp8 has been classified as Red List (Low Evidence).","entity_name":"FKBP8","entity_type":"gene"},{"created":"2022-01-21T10:46:32.043662+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2650","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FKBP8 were changed from Spina bifida, HP:0002414; Vertebral segmentation defects to Spina bifida, MONDO:0008449","entity_name":"FKBP8","entity_type":"gene"},{"created":"2022-01-21T10:45:59.516370+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2649","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FKBP8 as Red List (low evidence)","entity_name":"FKBP8","entity_type":"gene"},{"created":"2022-01-21T10:45:59.506339+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2649","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fkbp8 has been classified as Red List (Low Evidence).","entity_name":"FKBP8","entity_type":"gene"},{"created":"2022-01-21T10:45:04.151141+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10732","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ILK as ready","entity_name":"ILK","entity_type":"gene"},{"created":"2022-01-21T10:45:04.139575+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10732","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ilk has been classified as Red List (Low Evidence).","entity_name":"ILK","entity_type":"gene"},{"created":"2022-01-21T10:44:44.058835+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10732","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ILK were changed from  to Dilated cardiomyopathy","entity_name":"ILK","entity_type":"gene"},{"created":"2022-01-21T10:44:24.275543+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10731","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ILK were set to ","entity_name":"ILK","entity_type":"gene"},{"created":"2022-01-21T10:44:02.888326+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10730","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ILK was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ILK","entity_type":"gene"},{"created":"2022-01-21T10:43:44.306481+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10729","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ILK as Red List (low evidence)","entity_name":"ILK","entity_type":"gene"},{"created":"2022-01-21T10:43:44.294493+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10729","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ilk has been classified as Red List (Low Evidence).","entity_name":"ILK","entity_type":"gene"},{"created":"2022-01-21T10:43:22.077706+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10728","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ILK: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Dilated cardiomyopathy; Mode of inheritance: None","entity_name":"ILK","entity_type":"gene"},{"created":"2022-01-21T10:41:53.878491+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10728","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZIC4 as ready","entity_name":"ZIC4","entity_type":"gene"},{"created":"2022-01-21T10:41:53.874250+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10728","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Two individuals reported with a deletion of ZIC1 and ZIC4 and Dandy-Walker malformation.","entity_name":"ZIC4","entity_type":"gene"},{"created":"2022-01-21T10:41:53.833979+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10728","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zic4 has been classified as Red List (Low Evidence).","entity_name":"ZIC4","entity_type":"gene"},{"created":"2022-01-21T10:41:23.553565+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10728","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZIC4 were set to ","entity_name":"ZIC4","entity_type":"gene"},{"created":"2022-01-21T10:41:04.241410+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10727","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZIC4 as Red List (low evidence)","entity_name":"ZIC4","entity_type":"gene"},{"created":"2022-01-21T10:41:04.230031+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10727","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zic4 has been classified as Red List (Low Evidence).","entity_name":"ZIC4","entity_type":"gene"},{"created":"2022-01-21T10:40:26.837610+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.393","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZIC4 as ready","entity_name":"ZIC4","entity_type":"gene"},{"created":"2022-01-21T10:40:26.833618+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.393","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Two individuals with deletions of ZIC4 and ZIC1 reported with Dandy-Walker malformation.","entity_name":"ZIC4","entity_type":"gene"},{"created":"2022-01-21T10:40:26.797615+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.393","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zic4 has been classified as Red List (Low Evidence).","entity_name":"ZIC4","entity_type":"gene"},{"created":"2022-01-21T10:39:30.045554+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.393","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZIC4 were set to ","entity_name":"ZIC4","entity_type":"gene"},{"created":"2022-01-21T10:39:03.391729+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.392","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZIC4 as Red List (low evidence)","entity_name":"ZIC4","entity_type":"gene"},{"created":"2022-01-21T10:39:03.376975+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.392","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zic4 has been classified as Red List (Low Evidence).","entity_name":"ZIC4","entity_type":"gene"}]}