{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1464","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1462","results":[{"created":"2020-12-24T17:31:23.529669+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5798","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rbp4 has been classified as Green List (High Evidence).","entity_name":"RBP4","entity_type":"gene"},{"created":"2020-12-24T17:31:08.102284+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5798","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RBP4 were changed from  to Microphthalmia, isolated, with coloboma 10 MIM#616428; Retinal dystrophy, iris coloboma, and comedogenic acne syndrome MIM#615147","entity_name":"RBP4","entity_type":"gene"},{"created":"2020-12-24T17:30:48.275127+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5797","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RBP4 were set to ","entity_name":"RBP4","entity_type":"gene"},{"created":"2020-12-24T17:30:29.961436+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5796","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RBP4 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RBP4","entity_type":"gene"},{"created":"2020-12-24T17:30:10.928791+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5795","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RBP4: Rating: GREEN; Mode of pathogenicity: None; Publications: 25910211, 29178648, 23189188, 9888420, 32323592; Phenotypes: Microphthalmia, isolated, with coloboma 10 MIM#616428, Retinal dystrophy, iris coloboma, and comedogenic acne syndrome MIM#615147; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RBP4","entity_type":"gene"},{"created":"2020-12-24T17:28:12.576597+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RBP4 as ready","entity_name":"RBP4","entity_type":"gene"},{"created":"2020-12-24T17:28:12.567012+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rbp4 has been classified as Green List (High Evidence).","entity_name":"RBP4","entity_type":"gene"},{"created":"2020-12-24T17:26:58.395248+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.240","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VAX1 as ready","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:26:58.386716+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.240","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vax1 has been classified as Red List (Low Evidence).","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:26:50.978875+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.240","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VAX1 were changed from  to Microphthalmia, syndromic 11, MIM# 614402","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:26:21.560987+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.239","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VAX1 were set to ","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:25:48.706734+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.238","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VAX1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:24:13.717408+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.237","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VAX1 as Red List (low evidence)","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:24:13.708161+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.237","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vax1 has been classified as Red List (Low Evidence).","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:23:44.252804+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.236","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VAX1: Rating: RED; Mode of pathogenicity: None; Publications: 22095910; Phenotypes: Microphthalmia, syndromic 11, MIM# 614402; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:23:10.589369+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5795","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VAX1 as ready","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:23:10.581414+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5795","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vax1 has been classified as Red List (Low Evidence).","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:22:50.724741+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5795","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VAX1 were changed from  to Microphthalmia, syndromic 11, MIM# 614402","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:22:27.599504+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5794","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VAX1 were set to ","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:22:09.128310+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5793","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VAX1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:21:51.861521+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5792","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VAX1 as Red List (low evidence)","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:21:51.854082+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5792","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vax1 has been classified as Red List (Low Evidence).","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:21:34.143391+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5791","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VAX1: Rating: RED; Mode of pathogenicity: None; Publications: 22095910; Phenotypes: Microphthalmia, syndromic 11, MIM# 614402; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:20:50.683506+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VAX1 as ready","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:20:50.671513+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vax1 has been classified as Red List (Low Evidence).","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:20:42.569492+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VAX1 were changed from  to Microphthalmia, syndromic 11, MIM# 614402","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:20:15.283881+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VAX1 were set to ","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:19:49.154166+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VAX1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:19:23.569754+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VAX1 as Red List (low evidence)","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:19:23.559809+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vax1 has been classified as Red List (Low Evidence).","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:18:55.383193+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VAX1: Rating: RED; Mode of pathogenicity: None; Publications: 22095910; Phenotypes: Microphthalmia, syndromic 11, MIM# 614402; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VAX1","entity_type":"gene"},{"created":"2020-12-24T17:16:44.132716+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5791","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VSX2 as ready","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:16:44.120994+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5791","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vsx2 has been classified as Green List (High Evidence).","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:16:36.789475+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5791","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VSX2 were changed from  to Microphthalmia with coloboma 3, MIM# 610092; Microphthalmia, isolated 2, MIM# 610093","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:16:18.186792+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5790","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VSX2 were set to ","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:15:58.591915+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5789","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VSX2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:15:38.309932+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5788","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VSX2: Rating: GREEN; Mode of pathogenicity: None; Publications: 15257456, 17661825, 31884615, 28121235, 27301076, 24033328; Phenotypes: Microphthalmia with coloboma 3, MIM# 610092, Microphthalmia, isolated 2, MIM# 610093; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:14:21.792853+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VSX2 as ready","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:14:21.782322+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vsx2 has been classified as Green List (High Evidence).","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:14:18.552066+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VSX2 were changed from  to Microphthalmia with coloboma 3, MIM# 610092; Microphthalmia, isolated 2, MIM# 610093","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:13:55.925453+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VSX2 were set to ","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:12:30.887718+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VSX2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:12:00.333370+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VSX2: Rating: GREEN; Mode of pathogenicity: None; Publications: 15257456, 17661825, 31884615, 28121235, 27301076, 24033328; Phenotypes: Microphthalmia with coloboma 3, MIM# 610092, Microphthalmia, isolated 2, MIM# 610093; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VSX2","entity_type":"gene"},{"created":"2020-12-24T17:07:40.988428+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.986","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR37 as ready","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:07:40.976034+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.986","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr37 has been classified as Green List (High Evidence).","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:07:37.554961+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.986","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR37 were changed from  to Neurooculocardiogenitourinary syndrome, MIM# 618652","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:07:03.121050+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.985","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR37 were set to ","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:06:35.077325+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.984","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR37 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:06:04.954183+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.983","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR37: Rating: GREEN; Mode of pathogenicity: None; Publications: 31327508, 31327508; Phenotypes: Neurooculocardiogenitourinary syndrome, MIM# 618652; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:04:35.421815+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5788","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR37 as ready","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:04:35.409978+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5788","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr37 has been classified as Green List (High Evidence).","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:04:27.980410+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5788","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR37 were changed from  to Neurooculocardiogenitourinary syndrome, MIM# 618652","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:04:07.535764+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5787","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR37 were set to ","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:03:47.404465+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5786","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR37 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:03:29.546835+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5785","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR37: Rating: GREEN; Mode of pathogenicity: None; Publications: 31327508, 31327508; Phenotypes: Neurooculocardiogenitourinary syndrome, MIM# 618652; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:01:23.476270+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR37 as ready","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:01:23.465867+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr37 has been classified as Green List (High Evidence).","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:01:20.793176+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR37 were changed from  to Neurooculocardiogenitourinary syndrome, MIM# 618652","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:00:59.177578+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR37 were set to ","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:00:31.711396+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR37 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T17:00:01.294753+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WDR37: Rating: GREEN; Mode of pathogenicity: None; Publications: 31327508, 31327508; Phenotypes: Neurooculocardiogenitourinary syndrome, MIM# 618652; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WDR37","entity_type":"gene"},{"created":"2020-12-24T16:55:23.062139+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHD7 as ready","entity_name":"CHD7","entity_type":"gene"},{"created":"2020-12-24T16:55:23.051733+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chd7 has been classified as Green List (High Evidence).","entity_name":"CHD7","entity_type":"gene"},{"created":"2020-12-24T16:55:19.570592+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CHD7 were changed from  to CHARGE syndrome, MIM# 214800","entity_name":"CHD7","entity_type":"gene"},{"created":"2020-12-24T16:54:50.831447+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CHD7 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CHD7","entity_type":"gene"},{"created":"2020-12-24T16:54:22.977108+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CHD7: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: CHARGE syndrome, MIM# 214800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CHD7","entity_type":"gene"},{"created":"2020-12-24T16:53:16.990323+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BMP4 as ready","entity_name":"BMP4","entity_type":"gene"},{"created":"2020-12-24T16:53:16.982148+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bmp4 has been classified as Green List (High Evidence).","entity_name":"BMP4","entity_type":"gene"},{"created":"2020-12-24T16:53:14.490481+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BMP4 were changed from  to Microphthalmia, syndromic 6, MIM# 607932","entity_name":"BMP4","entity_type":"gene"},{"created":"2020-12-24T16:52:45.892336+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BMP4 were set to ","entity_name":"BMP4","entity_type":"gene"},{"created":"2020-12-24T16:52:18.076170+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BMP4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"BMP4","entity_type":"gene"},{"created":"2020-12-24T16:51:49.192138+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BMP4: Rating: GREEN; Mode of pathogenicity: None; Publications: 21340693, 31053785; Phenotypes: Microphthalmia, syndromic 6, MIM# 607932; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"BMP4","entity_type":"gene"},{"created":"2020-12-24T16:46:57.340108+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ASXL1 as ready","entity_name":"ASXL1","entity_type":"gene"},{"created":"2020-12-24T16:46:57.331683+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: asxl1 has been classified as Green List (High Evidence).","entity_name":"ASXL1","entity_type":"gene"},{"created":"2020-12-24T16:46:55.093182+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ASXL1 were changed from  to Bohring-Opitz syndrome , MIM#605039","entity_name":"ASXL1","entity_type":"gene"},{"created":"2020-12-24T16:46:26.577512+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ASXL1 were set to ","entity_name":"ASXL1","entity_type":"gene"},{"created":"2020-12-24T16:45:52.553228+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ASXL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ASXL1","entity_type":"gene"},{"created":"2020-12-24T16:45:21.244148+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ASXL1: Rating: GREEN; Mode of pathogenicity: None; Publications: 29446906; Phenotypes: Bohring-Opitz syndrome , MIM#605039; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ASXL1","entity_type":"gene"},{"created":"2020-12-24T16:41:47.220999+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALDH1A3 as ready","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:41:47.212483+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aldh1a3 has been classified as Green List (High Evidence).","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:41:42.480850+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALDH1A3 were changed from  to Microphthalmia, isolated 8, MIM# 615113","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:41:21.130204+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5785","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALDH1A3 as ready","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:41:21.122218+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5785","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aldh1a3 has been classified as Green List (High Evidence).","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:41:11.364203+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5785","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALDH1A3 were changed from  to Microphthalmia, isolated 8, MIM# 615113","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:40:53.746406+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5784","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALDH1A3 were set to ","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:40:29.887411+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5783","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALDH1A3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:40:11.945515+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5782","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ALDH1A3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23312594, 23591992, 30200890, 28890889, 26873617, 24777706; Phenotypes: Microphthalmia, isolated 8, MIM# 615113; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:40:05.598553+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALDH1A3 were set to ","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:39:46.440405+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALDH1A3 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:39:26.956650+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALDH1A3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T16:38:50.282838+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ALDH1A3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23312594, 23591992, 30200890, 28890889, 26873617, 24777706; Phenotypes: Microphthalmia, isolated 8, MIM# 615113; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALDH1A3","entity_type":"gene"},{"created":"2020-12-24T11:49:12.692248+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3338","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C16orf62 were changed from 3C/Ritscher-Schinzel-like syndrome to Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135","entity_name":"C16orf62","entity_type":"gene"},{"created":"2020-12-24T11:48:39.063242+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3337","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: C16orf62: Changed phenotypes: Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135","entity_name":"C16orf62","entity_type":"gene"},{"created":"2020-12-24T11:48:23.606984+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C16orf62 were changed from 3C/Ritscher-Schinzel-like syndrome to Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135","entity_name":"C16orf62","entity_type":"gene"},{"created":"2020-12-24T11:47:51.904380+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: C16orf62: Changed phenotypes: Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135","entity_name":"C16orf62","entity_type":"gene"},{"created":"2020-12-24T11:47:27.306275+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5782","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C16orf62 were changed from 3C/Ritscher-Schinzel-like syndrome to Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135","entity_name":"C16orf62","entity_type":"gene"},{"created":"2020-12-24T11:47:05.238016+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5781","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: C16orf62: Changed phenotypes: Ritscher-Schinzel syndrome-3 (RTSC3), MIM#619135","entity_name":"C16orf62","entity_type":"gene"},{"created":"2020-12-23T18:59:41.381869+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5781","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VEGFC as ready","entity_name":"VEGFC","entity_type":"gene"},{"created":"2020-12-23T18:59:41.370003+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5781","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vegfc has been classified as Green List (High Evidence).","entity_name":"VEGFC","entity_type":"gene"},{"created":"2020-12-23T18:59:33.927764+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5781","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VEGFC were changed from  to Lymphatic malformation 4, MIM#615907","entity_name":"VEGFC","entity_type":"gene"}]}