{"count":220732,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=973","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=971","results":[{"created":"2022-02-24T09:13:20.430867+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4104","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAZ as ready","entity_name":"TAZ","entity_type":"gene"},{"created":"2022-02-24T09:13:20.418583+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4104","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":"2022-02-24T09:13:15.988697+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4104","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAZ were changed from BARTH SYNDROME to Barth syndrome, MIM#302060","entity_name":"TAZ","entity_type":"gene"},{"created":"2022-02-24T09:13:03.727679+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4103","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TAZ were set to ","entity_name":"TAZ","entity_type":"gene"},{"created":"2022-02-24T09:12:22.333622+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4102","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBC1D20 as ready","entity_name":"TBC1D20","entity_type":"gene"},{"created":"2022-02-24T09:12:22.322081+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4102","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbc1d20 has been classified as Green List (High Evidence).","entity_name":"TBC1D20","entity_type":"gene"},{"created":"2022-02-24T09:12:18.423375+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4102","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBC1D20 were changed from Warburg micro syndrome 4; Warburg micro syndrome 4 615663 to Warburg micro syndrome 4, MIM# 615663","entity_name":"TBC1D20","entity_type":"gene"},{"created":"2022-02-24T09:11:25.394207+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4101","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBCD as ready","entity_name":"TBCD","entity_type":"gene"},{"created":"2022-02-24T09:11:25.384293+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4101","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbcd has been classified as Green List (High Evidence).","entity_name":"TBCD","entity_type":"gene"},{"created":"2022-02-24T09:11:18.325900+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4101","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBCD were set to ","entity_name":"TBCD","entity_type":"gene"},{"created":"2022-02-24T09:11:01.811723+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4100","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: CC abnormalities.; to: CC abnormalities, arthrogryposis are relevant to fetal panel.","entity_name":"TBCD","entity_type":"gene"},{"created":"2022-02-24T09:10:05.609241+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4100","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: TBCD: CC abnormalities.","entity_name":"TBCD","entity_type":"gene"},{"created":"2022-02-23T18:34:04.823056+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4100","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBX1 as ready","entity_name":"TBX1","entity_type":"gene"},{"created":"2022-02-23T18:34:04.813188+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4100","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbx1 has been classified as Green List (High Evidence).","entity_name":"TBX1","entity_type":"gene"},{"created":"2022-02-23T18:34:01.097398+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4100","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBX1 were changed from 22Q11.2 DELETION SYNDROME to DiGeorge syndrome, MIM# 188400","entity_name":"TBX1","entity_type":"gene"},{"created":"2022-02-23T18:33:47.822681+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4099","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBX1 were set to ","entity_name":"TBX1","entity_type":"gene"},{"created":"2022-02-23T18:33:36.303845+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4098","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: TBX1 was changed from  to None","entity_name":"TBX1","entity_type":"gene"},{"created":"2022-02-23T18:33:26.172820+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4097","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBX1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBX1","entity_type":"gene"},{"created":"2022-02-23T18:32:52.685626+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4096","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBX3 as ready","entity_name":"TBX3","entity_type":"gene"},{"created":"2022-02-23T18:32:52.673013+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4096","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbx3 has been classified as Green List (High Evidence).","entity_name":"TBX3","entity_type":"gene"},{"created":"2022-02-23T18:32:48.990009+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4096","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBX3 were changed from ULNAR-MAMMARY SYNDROME to Ulnar-mammary syndrome, MIM# 181450; MONDO:0008411","entity_name":"TBX3","entity_type":"gene"},{"created":"2022-02-23T18:32:36.886719+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4095","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBX3 were set to ","entity_name":"TBX3","entity_type":"gene"},{"created":"2022-02-23T18:32:25.166488+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4094","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBX3 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBX3","entity_type":"gene"},{"created":"2022-02-23T18:31:55.130089+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4093","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBX5 as ready","entity_name":"TBX5","entity_type":"gene"},{"created":"2022-02-23T18:31:55.119854+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4093","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbx5 has been classified as Green List (High Evidence).","entity_name":"TBX5","entity_type":"gene"},{"created":"2022-02-23T18:31:51.530299+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4093","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TBX5 were changed from HOLT-ORAM SYNDROME to Holt-Oram syndrome, MIM# 142900","entity_name":"TBX5","entity_type":"gene"},{"created":"2022-02-23T18:31:39.938531+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4092","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBX5 were set to ","entity_name":"TBX5","entity_type":"gene"},{"created":"2022-02-23T18:31:29.517148+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4091","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBX5 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBX5","entity_type":"gene"},{"created":"2022-02-23T18:30:59.734727+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4090","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCF4 as ready","entity_name":"TCF4","entity_type":"gene"},{"created":"2022-02-23T18:30:59.721848+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4090","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tcf4 has been classified as Green List (High Evidence).","entity_name":"TCF4","entity_type":"gene"},{"created":"2022-02-23T18:30:55.888608+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4090","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TCF4 were changed from PITT-HOPKINS SYNDROME to Pitt-Hopkins syndrome, MIM# 610954","entity_name":"TCF4","entity_type":"gene"},{"created":"2022-02-23T18:30:36.588500+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4089","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCF4 were set to ","entity_name":"TCF4","entity_type":"gene"},{"created":"2022-02-23T18:30:24.088760+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4088","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TCF4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TCF4","entity_type":"gene"},{"created":"2022-02-23T18:29:56.853631+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4087","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCIRG1 as ready","entity_name":"TCIRG1","entity_type":"gene"},{"created":"2022-02-23T18:29:56.843744+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4087","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tcirg1 has been classified as Green List (High Evidence).","entity_name":"TCIRG1","entity_type":"gene"},{"created":"2022-02-23T18:29:22.599262+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4087","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCTN1 as ready","entity_name":"TCTN1","entity_type":"gene"},{"created":"2022-02-23T18:29:22.587956+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4087","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tctn1 has been classified as Green List (High Evidence).","entity_name":"TCTN1","entity_type":"gene"},{"created":"2022-02-23T18:29:19.325821+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4087","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TCTN1 were changed from Joubert syndrome 13 614173; JOUBERT SYNDROME AND RELATED DISORDERS to Joubert syndrome 13, MIM# 614173","entity_name":"TCTN1","entity_type":"gene"},{"created":"2022-02-23T18:29:07.555395+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4086","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCTN1 were set to ","entity_name":"TCTN1","entity_type":"gene"},{"created":"2022-02-23T18:28:27.719936+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4085","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCTN2 as ready","entity_name":"TCTN2","entity_type":"gene"},{"created":"2022-02-23T18:28:27.696996+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4085","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tctn2 has been classified as Green List (High Evidence).","entity_name":"TCTN2","entity_type":"gene"},{"created":"2022-02-23T18:28:23.995872+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4085","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TCTN2 were changed from JOUBERT SYNDROME AND RELATED DISORDERS to Joubert syndrome 24, MIM# 616654; MONDO:0014724; Meckel syndrome 8, MIM# 613885; MONDO:0013482","entity_name":"TCTN2","entity_type":"gene"},{"created":"2022-02-23T18:28:14.987009+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4084","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCTN2 were set to 30712880","entity_name":"TCTN2","entity_type":"gene"},{"created":"2022-02-23T18:27:24.040295+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4083","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCTN3 as ready","entity_name":"TCTN3","entity_type":"gene"},{"created":"2022-02-23T18:27:24.031047+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4083","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tctn3 has been classified as Green List (High Evidence).","entity_name":"TCTN3","entity_type":"gene"},{"created":"2022-02-23T18:27:19.296412+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4083","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TCTN3 were changed from MOHR-MAJEWSKI SYNDROME to Joubert syndrome 18, OMIM #614815; Orofaciodigital syndrome IV, OMIM #258860","entity_name":"TCTN3","entity_type":"gene"},{"created":"2022-02-23T18:27:07.987906+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4082","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCTN3 were set to ","entity_name":"TCTN3","entity_type":"gene"},{"created":"2022-02-23T18:26:24.727546+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4081","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TFAP2A as ready","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2022-02-23T18:26:24.716664+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4081","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tfap2a has been classified as Green List (High Evidence).","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2022-02-23T18:23:10.688111+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4081","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TFAP2A were changed from BRANCHIOOCULOFACIAL SYNDROME to Branchiooculofacial syndrome, MIM# 113620","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2022-02-23T18:22:58.627841+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4080","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TFAP2A were set to ","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2022-02-23T18:22:47.483817+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4079","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TFAP2A was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2022-02-23T18:22:05.560436+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4078","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TFAP2B as ready","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:22:05.544370+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4078","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tfap2b has been classified as Green List (High Evidence).","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:21:42.675819+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4078","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TFAP2B were changed from CHAR SYNDROME to Char syndrome, MIM# 169100; Syndromic craniosynostosis","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:21:31.599161+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4077","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TFAP2B were set to ","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:21:20.835741+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4076","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TFAP2B was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:21:07.249869+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4075","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TFAP2B as Green List (high evidence)","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:21:07.239729+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4075","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tfap2b has been classified as Green List (High Evidence).","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:20:55.049751+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4074","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: PDA, facial dysmorphism and clinodactyly unlikely to be detectable antenatally.; to: Char syndrome: PDA, facial dysmorphism and clinodactyly unlikely to be detectable antenatally.\r\n\r\nCraniosynostosis: Four individuals reported in PMID: 31292255 (Correction in PMID: 31405973) as part of a craniosynostosis cohort: 2 de novo and 2 inherited. There is evidence for reduced penetrance as in one case the variant was inherited from an unaffected parent (affected parent for the other inherited variant). ","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:20:23.990881+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4074","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TFAP2B: Changed rating: GREEN; Changed publications: 31292255; Changed phenotypes: Char syndrome, MIM# 169100, Syndromic craniosynostosis","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:19:30.848098+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4074","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TFAP2B as Red List (low evidence)","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:19:30.835143+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4074","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tfap2b has been classified as Red List (Low Evidence).","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:19:17.384776+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4073","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TFAP2B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Char syndrome, MIM# 169100; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2022-02-23T18:17:00.366732+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4073","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFBR1 as ready","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2022-02-23T18:17:00.350923+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4073","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfbr1 has been classified as Green List (High Evidence).","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2022-02-23T18:16:01.758976+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4073","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGFBR1 were changed from LOEYS-DIETZ SYNDROME TYPE 2A; AORTIC ANEURYSM FAMILIAL THORACIC TYPE 5; LOEYS-DIETZ SYNDROME TYPE 1A to Loeys-Dietz syndrome 1, MIM# 609192","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2022-02-23T18:15:47.093829+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4072","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGFBR1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2022-02-23T18:15:34.982255+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4071","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TGFBR1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Loeys-Dietz syndrome 1, MIM# 609192; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2022-02-23T18:14:40.520251+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4071","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFBR2 as ready","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2022-02-23T18:14:40.510272+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4071","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfbr2 has been classified as Green List (High Evidence).","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2022-02-23T18:14:37.145249+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4071","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGFBR2 were changed from LOEYS-DIETZ SYNDROME; TGFBR2-RELATED LOEYS-DIETZ SYNDROME to Loeys-Dietz syndrome 2, MIM# 610168","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2022-02-23T18:14:16.790048+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4070","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGFBR2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2022-02-23T18:14:04.465838+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4069","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TGFBR2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Loeys-Dietz syndrome 2 610168; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2022-02-23T18:13:07.779572+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4069","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGIF1 as ready","entity_name":"TGIF1","entity_type":"gene"},{"created":"2022-02-23T18:13:07.766171+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4069","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgif1 has been classified as Green List (High Evidence).","entity_name":"TGIF1","entity_type":"gene"},{"created":"2022-02-23T18:13:01.412559+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4069","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGIF1 were changed from HOLOPROSENCEPHALY; Holoprosencephaly 4 142946 to Holoprosencephaly 4, MIM# 142946; MONDO:0007734","entity_name":"TGIF1","entity_type":"gene"},{"created":"2022-02-23T18:12:49.653766+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4068","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TGIF1 were set to ","entity_name":"TGIF1","entity_type":"gene"},{"created":"2022-02-23T18:12:38.154533+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4067","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGIF1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGIF1","entity_type":"gene"},{"created":"2022-02-23T18:12:07.809118+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4066","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TINF2 as ready","entity_name":"TINF2","entity_type":"gene"},{"created":"2022-02-23T18:12:07.798457+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4066","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tinf2 has been classified as Green List (High Evidence).","entity_name":"TINF2","entity_type":"gene"},{"created":"2022-02-23T18:12:04.190930+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4066","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TINF2 were changed from EXUDATIVE RETINOPATHY WITH BONE MARROW FAILURE to Revesz syndrome, MIM# 268130","entity_name":"TINF2","entity_type":"gene"},{"created":"2022-02-23T18:11:51.745294+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4065","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TINF2 were set to ","entity_name":"TINF2","entity_type":"gene"},{"created":"2022-02-23T18:11:39.962259+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4064","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TINF2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TINF2","entity_type":"gene"},{"created":"2022-02-23T18:11:28.194747+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4063","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Bone marrow failure is the main presenting feature. DD is part of the phenotype, neurological involvement progressive.; to: IUGR.","entity_name":"TINF2","entity_type":"gene"},{"created":"2022-02-23T18:10:48.274118+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4063","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM138 as ready","entity_name":"TMEM138","entity_type":"gene"},{"created":"2022-02-23T18:10:48.258048+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4063","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem138 has been classified as Green List (High Evidence).","entity_name":"TMEM138","entity_type":"gene"},{"created":"2022-02-23T18:10:44.652617+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4063","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM138 were changed from Joubert syndrome 16 614465 to Joubert syndrome 16, MIM# 614465; MONDO:0013764","entity_name":"TMEM138","entity_type":"gene"},{"created":"2022-02-23T18:10:32.766334+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4062","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM138 were set to ","entity_name":"TMEM138","entity_type":"gene"},{"created":"2022-02-23T18:10:04.193618+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4061","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM165 as ready","entity_name":"TMEM165","entity_type":"gene"},{"created":"2022-02-23T18:10:04.176268+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4061","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem165 has been classified as Green List (High Evidence).","entity_name":"TMEM165","entity_type":"gene"},{"created":"2022-02-23T18:09:56.600697+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4061","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM165 were changed from CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK to Congenital disorder of glycosylation, type IIk, MIM# 614727; TMEM165-CDG, MONDO:0013870","entity_name":"TMEM165","entity_type":"gene"},{"created":"2022-02-23T18:09:43.725290+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4060","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM165 were set to ","entity_name":"TMEM165","entity_type":"gene"},{"created":"2022-02-23T18:09:08.590871+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4059","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM231 as ready","entity_name":"TMEM231","entity_type":"gene"},{"created":"2022-02-23T18:09:08.577470+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4059","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem231 has been classified as Green List (High Evidence).","entity_name":"TMEM231","entity_type":"gene"},{"created":"2022-02-23T18:09:04.910684+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4059","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM231 were changed from Joubert syndrome 20 614970; Meckel syndrome 11 615397 to Joubert syndrome 20, MIM# 614970; MONDO:0013994; Meckel syndrome 11, MIM# 615397; MONDO:0014164","entity_name":"TMEM231","entity_type":"gene"},{"created":"2022-02-23T18:08:49.712607+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4058","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM231 were set to ","entity_name":"TMEM231","entity_type":"gene"},{"created":"2022-02-23T18:08:19.702999+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4057","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM237 as ready","entity_name":"TMEM237","entity_type":"gene"},{"created":"2022-02-23T18:08:19.692826+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4057","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem237 has been classified as Green List (High Evidence).","entity_name":"TMEM237","entity_type":"gene"},{"created":"2022-02-23T18:08:15.055704+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4057","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM237 were changed from JOUBERT SYNDROME 14 to Joubert syndrome 14, MIM# 614424","entity_name":"TMEM237","entity_type":"gene"}]}