{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=915","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=913","results":[{"created":"2022-03-26T09:30:04.017583+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11951","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBCK were set to ","entity_name":"TBCK","entity_type":"gene"},{"created":"2022-03-26T09:29:44.421514+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11950","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBCK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TBCK","entity_type":"gene"},{"created":"2022-03-26T09:29:26.747412+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11949","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TBCK: Rating: GREEN; Mode of pathogenicity: None; Publications: 27040692, 30103036, 27040691; Phenotypes: Hypotonia, infantile, with psychomotor retardation and characteristic facies 3, MIM# 616900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TBCK","entity_type":"gene"},{"created":"2022-03-26T09:13:08.417897+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4604","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBC1D23 as ready","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2022-03-26T09:13:08.407307+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4604","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbc1d23 has been classified as Green List (High Evidence).","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2022-03-26T09:13:04.290197+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4604","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBC1D23 were changed from  to Pontocerebellar hypoplasia, type 11, MIM# 617695","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2022-03-26T09:12:12.458166+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4603","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBC1D23 were set to ","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2022-03-26T09:11:30.369711+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4602","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBC1D23 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2022-03-26T09:10:56.803758+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4601","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TBC1D23: Rating: GREEN; Mode of pathogenicity: None; Publications: 28823707, 28823706; Phenotypes: Pontocerebellar hypoplasia, type 11, MIM# 617695; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2022-03-26T08:42:20.541788+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11949","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBC1D23 as ready","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2022-03-26T08:42:20.530663+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11949","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbc1d23 has been classified as Green List (High Evidence).","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2022-03-26T08:42:11.851898+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11949","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBC1D23 were changed from  to Pontocerebellar hypoplasia, type 11, MIM# 617695","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2022-03-26T08:41:52.173215+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11948","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBC1D23 were set to ","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2022-03-26T08:41:32.847926+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11947","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBC1D23 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TBC1D23","entity_type":"gene"},{"created":"2022-03-26T08:40:46.481148+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11946","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBC1D1 as ready","entity_name":"TBC1D1","entity_type":"gene"},{"created":"2022-03-26T08:40:46.469661+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11946","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbc1d1 has been classified as Green List (High Evidence).","entity_name":"TBC1D1","entity_type":"gene"},{"created":"2022-03-26T08:40:38.951473+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11946","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBC1D1 were changed from  to CAKUT; Non-syndromic renal or urinary tract malformation, MONDO:0019720","entity_name":"TBC1D1","entity_type":"gene"},{"created":"2022-03-26T08:40:20.801919+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11945","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBC1D1 were set to ","entity_name":"TBC1D1","entity_type":"gene"},{"created":"2022-03-26T08:40:00.515574+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11944","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBC1D1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBC1D1","entity_type":"gene"},{"created":"2022-03-26T08:39:39.303154+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11943","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TBC1D1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26572137; Phenotypes: CAKUT, Non-syndromic renal or urinary tract malformation, MONDO:0019720; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBC1D1","entity_type":"gene"},{"created":"2022-03-26T08:33:19.966210+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11943","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAZ as ready","entity_name":"TAZ","entity_type":"gene"},{"created":"2022-03-26T08:33:19.952671+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11943","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taz has been classified as Green List (High Evidence).","entity_name":"TAZ","entity_type":"gene"},{"created":"2022-03-26T08:33:10.215277+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11943","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAZ were changed from  to Barth syndrome, MIM# 302060","entity_name":"TAZ","entity_type":"gene"},{"created":"2022-03-26T08:32:47.589217+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11942","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAZ was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"TAZ","entity_type":"gene"},{"created":"2022-03-26T08:32:27.352506+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11941","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAZ: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Barth syndrome, MIM# 302060; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"TAZ","entity_type":"gene"},{"created":"2022-03-26T08:31:28.740805+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11941","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAT were changed from Tyrosinemia, type II, MIM# 276600 to Tyrosinaemia, type II, MIM# 276600","entity_name":"TAT","entity_type":"gene"},{"created":"2022-03-26T08:31:07.151555+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11940","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAT as ready","entity_name":"TAT","entity_type":"gene"},{"created":"2022-03-26T08:31:07.140139+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11940","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tat has been classified as Green List (High Evidence).","entity_name":"TAT","entity_type":"gene"},{"created":"2022-03-26T08:30:57.161853+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11940","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAT were changed from  to Tyrosinemia, type II, MIM# 276600","entity_name":"TAT","entity_type":"gene"},{"created":"2022-03-26T08:30:37.160730+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11939","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAT","entity_type":"gene"},{"created":"2022-03-26T08:29:44.637919+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11938","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAS2R38 as ready","entity_name":"TAS2R38","entity_type":"gene"},{"created":"2022-03-26T08:29:44.626715+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11938","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tas2r38 has been classified as Red List (Low Evidence).","entity_name":"TAS2R38","entity_type":"gene"},{"created":"2022-03-26T08:25:12.898531+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11938","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAS2R38 were changed from  to [Phenylthiocarbamide tasting] 171200","entity_name":"TAS2R38","entity_type":"gene"},{"created":"2022-03-26T08:24:52.356517+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11937","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAS2R38 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TAS2R38","entity_type":"gene"},{"created":"2022-03-26T08:23:42.557041+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11936","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAS2R38 as Red List (low evidence)","entity_name":"TAS2R38","entity_type":"gene"},{"created":"2022-03-26T08:23:42.544752+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11936","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tas2r38 has been classified as Red List (Low Evidence).","entity_name":"TAS2R38","entity_type":"gene"},{"created":"2022-03-26T08:23:23.704662+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11935","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAS2R38: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: [Phenylthiocarbamide tasting] 171200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TAS2R38","entity_type":"gene"},{"created":"2022-03-26T08:22:32.757450+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11935","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAS2R16 as ready","entity_name":"TAS2R16","entity_type":"gene"},{"created":"2022-03-26T08:22:32.746574+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11935","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tas2r16 has been classified as Red List (Low Evidence).","entity_name":"TAS2R16","entity_type":"gene"},{"created":"2022-03-26T08:22:23.460353+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11935","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAS2R16 were changed from  to [Beta-glycopyranoside tasting], (3) {Alcohol dependence, susceptibility to} 617956","entity_name":"TAS2R16","entity_type":"gene"},{"created":"2022-03-26T08:22:03.533806+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11934","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAS2R16 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TAS2R16","entity_type":"gene"},{"created":"2022-03-26T08:21:45.293968+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11933","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAS2R16 as Red List (low evidence)","entity_name":"TAS2R16","entity_type":"gene"},{"created":"2022-03-26T08:21:45.282615+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11933","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tas2r16 has been classified as Red List (Low Evidence).","entity_name":"TAS2R16","entity_type":"gene"},{"created":"2022-03-26T08:21:26.996309+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11932","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAS2R16: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: [Beta-glycopyranoside tasting], (3) {Alcohol dependence, susceptibility to} 617956; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TAS2R16","entity_type":"gene"},{"created":"2022-03-25T23:21:54.109915+11:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.246","user_name":"Arina Puzriakova","item_type":"entity","text":"reviewed gene: ACER3: Rating: GREEN; Mode of pathogenicity: None; Publications: 34281620; Phenotypes: Leukodystrophy, progressive, early childhood-onset, OMIM:617762; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACER3","entity_type":"gene"},{"created":"2022-03-25T18:57:01.827333+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11932","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TANGO2 as ready","entity_name":"TANGO2","entity_type":"gene"},{"created":"2022-03-25T18:57:01.815011+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11932","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tango2 has been classified as Green List (High Evidence).","entity_name":"TANGO2","entity_type":"gene"},{"created":"2022-03-25T18:56:53.999109+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11932","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TANGO2 were changed from  to Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration, MIM# 616878","entity_name":"TANGO2","entity_type":"gene"},{"created":"2022-03-25T18:56:35.723955+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11931","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TANGO2 were set to ","entity_name":"TANGO2","entity_type":"gene"},{"created":"2022-03-25T18:56:12.664905+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11930","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TANGO2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TANGO2","entity_type":"gene"},{"created":"2022-03-25T15:31:42.854789+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11929","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TANGO2: Rating: GREEN; Mode of pathogenicity: None; Publications: 26805782, 30245509; Phenotypes: Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration, MIM# 616878; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TANGO2","entity_type":"gene"},{"created":"2022-03-25T15:29:13.374812+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11929","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TACR3 as ready","entity_name":"TACR3","entity_type":"gene"},{"created":"2022-03-25T15:29:13.364902+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11929","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tacr3 has been classified as Green List (High Evidence).","entity_name":"TACR3","entity_type":"gene"},{"created":"2022-03-25T15:29:04.991812+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11929","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TACR3 were changed from  to Hypogonadotropic hypogonadism 11 with or without anosmia, MIM# 614840","entity_name":"TACR3","entity_type":"gene"},{"created":"2022-03-25T15:28:43.333362+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11928","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TACR3 were set to ","entity_name":"TACR3","entity_type":"gene"},{"created":"2022-03-25T15:28:23.154355+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11927","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TACR3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TACR3","entity_type":"gene"},{"created":"2022-03-25T15:28:00.338417+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11926","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TACR3: Rating: GREEN; Mode of pathogenicity: None; Publications: 20332248, 19079066; Phenotypes: Hypogonadotropic hypogonadism 11 with or without anosmia, MIM# 614840; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TACR3","entity_type":"gene"},{"created":"2022-03-25T15:24:28.279349+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11926","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAC3 as ready","entity_name":"TAC3","entity_type":"gene"},{"created":"2022-03-25T15:24:28.267736+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11926","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tac3 has been classified as Green List (High Evidence).","entity_name":"TAC3","entity_type":"gene"},{"created":"2022-03-25T15:24:19.117015+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11926","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAC3 were changed from  to Hypogonadotropic hypogonadism 10 with or without anosmia, MIM# 614839","entity_name":"TAC3","entity_type":"gene"},{"created":"2022-03-25T15:22:17.148007+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11925","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TAC3 were set to ","entity_name":"TAC3","entity_type":"gene"},{"created":"2022-03-25T15:21:57.053909+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11924","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TAC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAC3","entity_type":"gene"},{"created":"2022-03-25T15:21:38.150217+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11923","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TAC3: Rating: GREEN; Mode of pathogenicity: None; Publications: 19079066, 20332248, 23329188, 22031817; Phenotypes: Hypogonadotropic hypogonadism 10 with or without anosmia, MIM# 614839; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAC3","entity_type":"gene"},{"created":"2022-03-25T15:19:51.571111+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11923","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: T as ready","entity_name":"T","entity_type":"gene"},{"created":"2022-03-25T15:19:51.558097+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11923","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: t has been classified as Red List (Low Evidence).","entity_name":"T","entity_type":"gene"},{"created":"2022-03-25T15:18:25.727710+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11923","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: T were changed from  to Sacral agenesis with vertebral anomalies, MIM# 615709","entity_name":"T","entity_type":"gene"},{"created":"2022-03-25T15:18:02.319693+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11922","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: T were set to ","entity_name":"T","entity_type":"gene"},{"created":"2022-03-25T15:17:42.661174+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11921","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: T was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"T","entity_type":"gene"},{"created":"2022-03-25T15:17:23.013098+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11920","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: T as Red List (low evidence)","entity_name":"T","entity_type":"gene"},{"created":"2022-03-25T15:17:23.001264+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11920","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: t has been classified as Red List (Low Evidence).","entity_name":"T","entity_type":"gene"},{"created":"2022-03-25T14:56:52.624942+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11919","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: T: Rating: RED; Mode of pathogenicity: None; Publications: 24253444, 28116192; Phenotypes: Sacral agenesis with vertebral anomalies 615709; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"T","entity_type":"gene"},{"created":"2022-03-25T14:52:18.530906+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11919","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LAT were set to ","entity_name":"LAT","entity_type":"gene"},{"created":"2022-03-25T14:51:27.911472+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.238","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EPHB4 as ready","entity_name":"EPHB4","entity_type":"gene"},{"created":"2022-03-25T14:51:27.900498+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.238","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ephb4 has been classified as Green List (High Evidence).","entity_name":"EPHB4","entity_type":"gene"},{"created":"2022-03-25T14:16:29.944101+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.238","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EPHB4 were changed from  to Lymphatic malformation 7 (MIM#617300), AD","entity_name":"EPHB4","entity_type":"gene"},{"created":"2022-03-25T14:15:56.842892+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.237","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EPHB4 were set to ","entity_name":"EPHB4","entity_type":"gene"},{"created":"2022-03-25T14:15:03.323133+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.236","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EPHB4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EPHB4","entity_type":"gene"},{"created":"2022-03-25T14:14:03.232068+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.235","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GUSB as ready","entity_name":"GUSB","entity_type":"gene"},{"created":"2022-03-25T14:14:03.220802+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.235","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gusb has been classified as Green List (High Evidence).","entity_name":"GUSB","entity_type":"gene"},{"created":"2022-03-25T14:13:54.176832+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.235","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GUSB were changed from  to Mucopolysaccharidosis VII, MIM# 253220; MONDO:0009662","entity_name":"GUSB","entity_type":"gene"},{"created":"2022-03-25T14:13:31.588795+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.234","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GUSB were set to ","entity_name":"GUSB","entity_type":"gene"},{"created":"2022-03-25T14:12:58.891907+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.233","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GUSB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GUSB","entity_type":"gene"},{"created":"2022-03-25T14:12:28.845707+11:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.232","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GUSB: Rating: GREEN; Mode of pathogenicity: None; Publications: 34302381; Phenotypes: Mucopolysaccharidosis VII, MIM# 253220, MONDO:0009662; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GUSB","entity_type":"gene"},{"created":"2022-03-25T14:10:40.367345+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11918","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCF20 were set to 30739909; 30819258; 25228304","entity_name":"TCF20","entity_type":"gene"},{"created":"2022-03-25T14:08:46.192899+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11917","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LAS1L were set to 25644381; 34653234; 26358559","entity_name":"LAS1L","entity_type":"gene"},{"created":"2022-03-25T14:07:06.874569+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11916","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: LAS1L: Changed rating: GREEN; Changed phenotypes: Wilson-Turner syndrome, MIM# 309585, congenital lethal motor neuron disease","entity_name":"LAS1L","entity_type":"gene"},{"created":"2022-03-25T14:06:17.806229+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11916","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LARGE1 were set to ","entity_name":"LARGE1","entity_type":"gene"},{"created":"2022-03-25T14:05:53.123142+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11915","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LARGE1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LARGE1","entity_type":"gene"},{"created":"2022-03-25T14:05:10.474177+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMC3 as ready","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:05:10.459974+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamc3 has been classified as Green List (High Evidence).","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:05:07.605851+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LAMC3 were changed from  to Cortical malformations, occipital, MIM#614115","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:03:54.964492+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LAMC3 were set to ","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:03:23.784439+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LAMC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:02:53.785532+11:00","panel_name":"Polymicrogyria and Schizencephaly","panel_id":18,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LAMC3: Rating: GREEN; Mode of pathogenicity: None; Publications: 21572413, 34354730; Phenotypes: Cortical malformations, occipital, MIM#614115; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:02:37.590867+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11914","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LAMC3 were changed from  to Cortical malformations, occipital, MIM#614115","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:02:12.805026+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1508","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMC3 as ready","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:02:12.793681+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1508","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamc3 has been classified as Green List (High Evidence).","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:02:07.978154+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1508","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LAMC3 as Green List (high evidence)","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:02:07.967971+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1508","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lamc3 has been classified as Green List (High Evidence).","entity_name":"LAMC3","entity_type":"gene"},{"created":"2022-03-25T14:01:18.280517+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11913","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LAMC3 were set to ","entity_name":"LAMC3","entity_type":"gene"}]}