{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1462","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1460","results":[{"created":"2020-12-28T14:35:53.791043+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5823","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RARB was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RARB","entity_type":"gene"},{"created":"2020-12-28T14:35:34.386275+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5822","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RARB: Rating: GREEN; Mode of pathogenicity: Other; Publications: 30880327, 30281527, 24075189, 27120018, 25457163, 17506106; Phenotypes: Microphthalmia, syndromic 12, MIM# 615524; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RARB","entity_type":"gene"},{"created":"2020-12-28T14:34:36.559172+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RARB as ready","entity_name":"RARB","entity_type":"gene"},{"created":"2020-12-28T14:34:36.548676+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rarb has been classified as Green List (High Evidence).","entity_name":"RARB","entity_type":"gene"},{"created":"2020-12-28T14:34:34.538878+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RARB were changed from  to Microphthalmia, syndromic 12, MIM# 615524","entity_name":"RARB","entity_type":"gene"},{"created":"2020-12-28T14:34:07.118365+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RARB were set to ","entity_name":"RARB","entity_type":"gene"},{"created":"2020-12-28T14:33:37.353309+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: RARB was changed from  to Other","entity_name":"RARB","entity_type":"gene"},{"created":"2020-12-28T14:32:19.387339+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RARB was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RARB","entity_type":"gene"},{"created":"2020-12-28T14:31:48.305981+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RARB: Rating: GREEN; Mode of pathogenicity: Other; Publications: 30880327, 30281527, 24075189, 27120018, 25457163, 17506106; Phenotypes: Microphthalmia, syndromic 12, MIM# 615524; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RARB","entity_type":"gene"},{"created":"2020-12-28T14:28:16.753749+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5822","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RARA were changed from  to Syndromic chorioretinal coloboma","entity_name":"RARA","entity_type":"gene"},{"created":"2020-12-28T14:27:59.010138+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5821","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RARA were set to ","entity_name":"RARA","entity_type":"gene"},{"created":"2020-12-28T14:27:44.380317+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5820","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RARA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RARA","entity_type":"gene"},{"created":"2020-12-28T14:27:23.796648+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5819","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"RARA","entity_type":"gene"},{"created":"2020-12-28T14:27:16.719301+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5819","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RARA: Added comment: Single case report of de novo missense variant in association with syndromic coloboma.; Changed publications: 31343737; Changed phenotypes: Syndromic chorioretinal coloboma","entity_name":"RARA","entity_type":"gene"},{"created":"2020-12-28T14:23:35.411053+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.254","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB3GAP2 as ready","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:23:35.402791+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.254","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab3gap2 has been classified as Green List (High Evidence).","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:23:29.398529+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.254","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB3GAP2 were changed from  to Warburg micro syndrome 2, MIM# 614225","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:23:01.390350+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.253","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB3GAP2 were set to ","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:22:33.331222+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.252","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAB3GAP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:22:01.221630+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.251","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Multiple families reported, well established gene-disease association.; to: Multiple families reported, well established gene-disease association. Cataract is a feature.","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:21:52.205606+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.251","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RAB3GAP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23420520, 20967465; Phenotypes: Warburg micro syndrome 2, MIM# 614225; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:21:20.307076+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.190","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB3GAP2 as ready","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:21:20.297679+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.190","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab3gap2 has been classified as Green List (High Evidence).","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:21:16.644889+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.190","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB3GAP2 were changed from Warburg micro syndrome to Warburg micro syndrome 2, MIM# 614225","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:21:05.134192+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.189","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB3GAP2 were set to ","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:20:54.795212+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.188","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RAB3GAP2 as Green List (high evidence)","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:20:54.787253+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.188","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab3gap2 has been classified as Green List (High Evidence).","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:20:42.670993+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.187","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RAB3GAP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23420520, 20967465; Phenotypes: Warburg micro syndrome 2, MIM# 614225; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:19:47.782699+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB3GAP2 as ready","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:19:47.772241+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab3gap2 has been classified as Green List (High Evidence).","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:19:44.981544+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB3GAP2 were changed from  to Warburg micro syndrome 2, MIM# 614225","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:18:42.470743+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB3GAP2 were set to ","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:18:15.143212+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAB3GAP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:17:43.747204+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RAB3GAP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23420520, 20967465; Phenotypes: Warburg micro syndrome 2, MIM# 614225; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2020-12-28T14:17:08.440555+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.251","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB3GAP1 were changed from Warburg micro syndrome 1, MIM# 600118 to Warburg micro syndrome 1, MIM# 600118","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:16:53.309372+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.251","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB3GAP1 as ready","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:16:53.273570+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.251","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab3gap1 has been classified as Green List (High Evidence).","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:16:48.083303+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.251","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB3GAP1 were changed from  to Warburg micro syndrome 1, MIM# 600118","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:16:20.876415+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.250","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB3GAP1 were set to ","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:15:52.083572+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.249","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAB3GAP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:15:51.296926+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB3GAP1 as ready","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:15:51.286424+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab3gap1 has been classified as Green List (High Evidence).","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:15:27.903703+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB3GAP1 were changed from  to Warburg micro syndrome 1, MIM# 600118","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:15:22.699216+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.248","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RAB3GAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 15696165, 20512159, 23420520; Phenotypes: Warburg micro syndrome 1, MIM# 600118; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:14:54.875447+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB3GAP1 were set to ","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:14:26.221950+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAB3GAP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:13:57.215656+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Rare autosomal recessive syndrome characterized by microcephaly, microphthalmia, microcornea, congenital cataracts, optic atrophy, cortical dysplasia, in particular corpus callosum hypoplasia, severe mental retardation, spastic diplegia, and hypogonadism. Multiple families reported.; to: Rare autosomal recessive syndrome characterized by microcephaly, microphthalmia, microcornea, congenital cataracts, optic atrophy, cortical dysplasia, in particular corpus callosum hypoplasia, severe ID, spastic diplegia, and hypogonadism. Multiple families reported.","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T14:13:46.245670+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RAB3GAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 15696165, 20512159, 23420520; Phenotypes: Warburg micro syndrome 1, MIM# 600118; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2020-12-28T10:31:47.825061+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5819","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PXDN as ready","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:31:47.815104+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5819","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pxdn has been classified as Green List (High Evidence).","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:31:35.814574+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5819","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PXDN were changed from  to Anterior segment dysgenesis 7, with sclerocornea, MIM# 269400","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:31:19.362269+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5818","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PXDN were set to ","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:30:58.103160+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5817","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PXDN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:30:34.608306+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5816","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PXDN: Rating: GREEN; Mode of pathogenicity: None; Publications: 21907015, 24939590, 32499604, 32224865, 32015378, 31817535; Phenotypes: Anterior segment dysgenesis 7, with sclerocornea, MIM# 269400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:29:57.154006+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.248","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PXDN as ready","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:29:57.146297+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.248","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pxdn has been classified as Green List (High Evidence).","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:29:54.188821+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.248","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PXDN were changed from  to Anterior segment dysgenesis 7, with sclerocornea, MIM# 269400","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:29:26.604823+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.247","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PXDN were set to ","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:28:57.465975+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.246","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PXDN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:28:29.221228+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.245","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PXDN: Rating: GREEN; Mode of pathogenicity: None; Publications: 21907015, 24939590, 32499604, 32224865, 32015378, 31817535; Phenotypes: Anterior segment dysgenesis 7, with sclerocornea, MIM# 269400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:27:49.745808+11:00","panel_name":"Eye Anterior Segment Abnormalities","panel_id":43,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PXDN as ready","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:27:49.737549+11:00","panel_name":"Eye Anterior Segment Abnormalities","panel_id":43,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pxdn has been classified as Green List (High Evidence).","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:27:47.298243+11:00","panel_name":"Eye Anterior Segment Abnormalities","panel_id":43,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PXDN were changed from  to Anterior segment dysgenesis 7, with sclerocornea, MIM# 269400","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:27:19.730258+11:00","panel_name":"Eye Anterior Segment Abnormalities","panel_id":43,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PXDN were set to ","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:26:54.719789+11:00","panel_name":"Eye Anterior Segment Abnormalities","panel_id":43,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PXDN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:26:25.050550+11:00","panel_name":"Eye Anterior Segment Abnormalities","panel_id":43,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PXDN: Rating: GREEN; Mode of pathogenicity: None; Publications: 21907015, 24939590, 32499604, 32224865, 32015378, 31817535; Phenotypes: Anterior segment dysgenesis 7, with sclerocornea, MIM# 269400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:25:36.165862+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PXDN as ready","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:25:36.154767+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pxdn has been classified as Green List (High Evidence).","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:25:32.538652+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PXDN were changed from  to Anterior segment dysgenesis 7, with sclerocornea, MIM# 269400","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:25:10.308378+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PXDN were set to ","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:24:48.536241+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PXDN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:24:20.179273+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PXDN: Rating: GREEN; Mode of pathogenicity: None; Publications: 21907015, 24939590, 32499604, 32224865, 32015378, 31817535; Phenotypes: Anterior segment dysgenesis 7, with sclerocornea, MIM# 269400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PXDN","entity_type":"gene"},{"created":"2020-12-28T10:20:10.381150+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PAX6 as ready","entity_name":"PAX6","entity_type":"gene"},{"created":"2020-12-28T10:20:10.370337+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pax6 has been classified as Green List (High Evidence).","entity_name":"PAX6","entity_type":"gene"},{"created":"2020-12-28T10:20:06.713988+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PAX6 were changed from  to Microphthalmia; Coloboma, ocular, MIM# 120200","entity_name":"PAX6","entity_type":"gene"},{"created":"2020-12-28T10:19:37.093944+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PAX6 were set to ","entity_name":"PAX6","entity_type":"gene"},{"created":"2020-12-28T10:19:07.562845+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PAX6 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PAX6","entity_type":"gene"},{"created":"2020-12-28T10:18:37.298130+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PAX6: Rating: GREEN; Mode of pathogenicity: None; Publications: 31700164, 30986449, 29930474, 22171686; Phenotypes: Microphthalmia, Coloboma, ocular, MIM# 120200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PAX6","entity_type":"gene"},{"created":"2020-12-28T09:27:10.191922+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PAX2 as ready","entity_name":"PAX2","entity_type":"gene"},{"created":"2020-12-28T09:27:10.180015+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pax2 has been classified as Green List (High Evidence).","entity_name":"PAX2","entity_type":"gene"},{"created":"2020-12-28T09:27:07.725506+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PAX2 were changed from  to Papillorenal syndrome, MIM# 120330; Renal coloboma syndrome, MONDO:0007352","entity_name":"PAX2","entity_type":"gene"},{"created":"2020-12-28T09:26:39.579371+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PAX2 were set to ","entity_name":"PAX2","entity_type":"gene"},{"created":"2020-12-28T09:26:10.699188+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PAX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PAX2","entity_type":"gene"},{"created":"2020-12-28T09:25:39.087180+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PAX2: Rating: GREEN; Mode of pathogenicity: None; Publications: 21654726; Phenotypes: Papillorenal syndrome, MIM# 120330, Renal coloboma syndrome, MONDO:0007352; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PAX2","entity_type":"gene"},{"created":"2020-12-27T16:09:32.678406+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3347","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMOC1 as ready","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:09:32.651700+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3347","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smoc1 has been classified as Green List (High Evidence).","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:09:23.079574+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3347","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMOC1 were changed from  to Microphthalmia with limb anomalies, MIM# 206920","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:08:52.359386+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3346","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMOC1 were set to ","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:08:19.278975+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3345","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMOC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:07:47.442247+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3344","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMOC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 21194678, 21194680, 30445150; Phenotypes: Microphthalmia with limb anomalies, MIM# 206920; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:05:28.839066+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMOC1 as ready","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:05:28.828349+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smoc1 has been classified as Green List (High Evidence).","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:05:12.636509+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMOC1 were changed from  to Microphthalmia with limb anomalies, MIM# 206920","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:04:43.491069+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5816","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMOC1 as ready","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:04:43.479677+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5816","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smoc1 has been classified as Green List (High Evidence).","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:04:35.860237+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5816","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMOC1 were changed from  to Microphthalmia with limb anomalies, MIM# 206920","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:04:16.663344+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5815","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMOC1 were set to ","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:03:58.879106+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5814","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMOC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:03:45.497143+11:00","panel_name":"Anophthalmia_Microphthalmia_Coloboma","panel_id":42,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMOC1 were set to ","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-12-27T16:03:31.664374+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5813","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMOC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 21194678, 21194680, 30445150; Phenotypes: Microphthalmia with limb anomalies, MIM# 206920; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMOC1","entity_type":"gene"}]}