{"count":220463,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=75","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=73","results":[{"created":"2025-12-24T18:09:36.505756+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.509","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VIM were changed from  to Cataract 30, pulverulent, MIM# 116300","entity_name":"VIM","entity_type":"gene"},{"created":"2025-12-24T18:09:14.941043+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.508","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VIM were set to ","entity_name":"VIM","entity_type":"gene"},{"created":"2025-12-24T18:08:54.309887+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.507","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VIM was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VIM","entity_type":"gene"},{"created":"2025-12-24T18:08:28.483518+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.506","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VIM: Rating: GREEN; Mode of pathogenicity: None; Publications: 26694549; Phenotypes: Cataract 30, pulverulent, MIM# 116300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VIM","entity_type":"gene"},{"created":"2025-12-24T18:05:45.251580+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.506","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TFAP2A as ready","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2025-12-24T18:05:45.243099+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.506","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":"2025-12-24T18:05:42.548157+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.506","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TFAP2A were changed from  to Branchiooculofacial syndrome, MIM# 113620","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2025-12-24T18:05:02.976610+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.505","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TFAP2A were set to ","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2025-12-24T18:04:37.040012+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.504","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TFAP2A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2025-12-24T18:04:14.073558+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.503","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TFAP2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 36263936; Phenotypes: Branchiooculofacial syndrome, MIM# 113620; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2025-12-24T17:37:01.125505+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.503","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC2A1 as ready","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2025-12-24T17:37:01.118015+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc2a1 has been classified as Green List (High Evidence).","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2025-12-24T17:36:58.797610+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.503","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC2A1 were changed from  to GLUT1 deficiency syndrome MONDO:0000188; Stomatin-deficient cryohydrocytosis with neurologic defects, MIM# 608885","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2025-12-24T17:36:37.447168+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.502","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC2A1 were set to ","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2025-12-24T17:36:13.085419+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.501","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC2A1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2025-12-24T17:35:13.837531+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.500","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC2A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22492876; Phenotypes: GLUT1 deficiency syndrome MONDO:0000188, Stomatin-deficient cryohydrocytosis with neurologic defects, MIM# 608885; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SLC2A1","entity_type":"gene"},{"created":"2025-12-24T17:31:21.724197+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.500","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PITX3 as ready","entity_name":"PITX3","entity_type":"gene"},{"created":"2025-12-24T17:31:21.714026+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.500","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pitx3 has been classified as Green List (High Evidence).","entity_name":"PITX3","entity_type":"gene"},{"created":"2025-12-24T17:31:18.944295+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.500","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PITX3 were changed from  to Anterior segment dysgenesis 1, multiple subtypes, MIM# 107250 Cataract 11, multiple types, MIM# 610623","entity_name":"PITX3","entity_type":"gene"},{"created":"2025-12-24T17:30:53.604261+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.499","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PITX3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PITX3","entity_type":"gene"},{"created":"2025-12-24T17:30:27.051966+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.498","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PITX3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Anterior segment dysgenesis 1, multiple subtypes, MIM# 107250 Cataract 11, multiple types, MIM# 610623; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PITX3","entity_type":"gene"},{"created":"2025-12-24T17:29:39.782521+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.498","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX7 as ready","entity_name":"PEX7","entity_type":"gene"},{"created":"2025-12-24T17:29:39.775396+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.498","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex7 has been classified as Green List (High Evidence).","entity_name":"PEX7","entity_type":"gene"},{"created":"2025-12-24T17:29:36.385890+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.498","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX7 were changed from  to Peroxisome biogenesis disorder 2A (Zellweger), MIM# 214110","entity_name":"PEX7","entity_type":"gene"},{"created":"2025-12-24T17:29:15.367922+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.497","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX7","entity_type":"gene"},{"created":"2025-12-24T17:28:47.567830+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.496","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX7: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 2A (Zellweger), MIM# 214110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX7","entity_type":"gene"},{"created":"2025-12-24T17:27:51.888485+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.496","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX6 as ready","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-12-24T17:27:51.880562+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.496","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex6 has been classified as Green List (High Evidence).","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-12-24T17:27:48.972390+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.496","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX6 were changed from  to Peroxisome biogenesis disorder 4A (Zellweger) (MIM#614862)","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-12-24T17:27:22.542865+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.495","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-12-24T17:26:55.393889+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.494","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX6: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 4A (Zellweger) (MIM#614862); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-12-24T17:26:23.420743+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.494","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX5 as ready","entity_name":"PEX5","entity_type":"gene"},{"created":"2025-12-24T17:26:23.410050+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.494","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex5 has been classified as Green List (High Evidence).","entity_name":"PEX5","entity_type":"gene"},{"created":"2025-12-24T17:26:20.794958+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.494","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX5 were changed from  to Peroxisome biogenesis disorder 2A (Zellweger) (MIM#214110)","entity_name":"PEX5","entity_type":"gene"},{"created":"2025-12-24T17:25:54.867576+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.493","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX5","entity_type":"gene"},{"created":"2025-12-24T17:25:32.687938+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.492","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX5: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 2A (Zellweger) (MIM#214110); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX5","entity_type":"gene"},{"created":"2025-12-24T17:25:00.410689+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.492","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX3 as ready","entity_name":"PEX3","entity_type":"gene"},{"created":"2025-12-24T17:25:00.398915+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.492","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex3 has been classified as Green List (High Evidence).","entity_name":"PEX3","entity_type":"gene"},{"created":"2025-12-24T17:24:57.609944+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.492","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX3 were changed from  to Peroxisome biogenesis disorder 10A (Zellweger) 614882","entity_name":"PEX3","entity_type":"gene"},{"created":"2025-12-24T17:24:31.813734+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.491","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX3","entity_type":"gene"},{"created":"2025-12-24T17:24:04.315672+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.490","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 10A (Zellweger) 614882; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX3","entity_type":"gene"},{"created":"2025-12-24T16:10:53.189071+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.490","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX26 as ready","entity_name":"PEX26","entity_type":"gene"},{"created":"2025-12-24T16:10:53.179646+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.490","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex26 has been classified as Green List (High Evidence).","entity_name":"PEX26","entity_type":"gene"},{"created":"2025-12-24T16:10:50.438754+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.490","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX26 were changed from  to Peroxisome biogenesis disorder 7A (Zellweger) MIM#614872","entity_name":"PEX26","entity_type":"gene"},{"created":"2025-12-24T16:10:26.900309+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.489","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX26 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX26","entity_type":"gene"},{"created":"2025-12-24T16:09:57.464154+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.488","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX26: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 7A (Zellweger) MIM#614872; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX26","entity_type":"gene"},{"created":"2025-12-24T16:09:18.836194+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.488","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX2 as ready","entity_name":"PEX2","entity_type":"gene"},{"created":"2025-12-24T16:09:18.826617+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.488","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex2 has been classified as Green List (High Evidence).","entity_name":"PEX2","entity_type":"gene"},{"created":"2025-12-24T16:09:16.770674+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.488","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX2 were changed from  to Peroxisome biogenesis disorder 5A (Zellweger) MIM#614866","entity_name":"PEX2","entity_type":"gene"},{"created":"2025-12-24T16:08:47.292498+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.487","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX2","entity_type":"gene"},{"created":"2025-12-24T16:08:21.786692+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.486","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 5A (Zellweger) MIM#614866; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX2","entity_type":"gene"},{"created":"2025-12-24T16:07:42.623218+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX19 as ready","entity_name":"PEX19","entity_type":"gene"},{"created":"2025-12-24T16:07:42.616559+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.486","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex19 has been classified as Green List (High Evidence).","entity_name":"PEX19","entity_type":"gene"},{"created":"2025-12-24T16:07:39.798861+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.486","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX19 were changed from  to Peroxisome biogenesis disorder 12A (Zellweger) MIM#614886","entity_name":"PEX19","entity_type":"gene"},{"created":"2025-12-24T16:07:13.690913+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.485","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX19 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX19","entity_type":"gene"},{"created":"2025-12-24T16:06:50.079738+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.484","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX19: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 12A (Zellweger) MIM#614886; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX19","entity_type":"gene"},{"created":"2025-12-24T16:06:09.751951+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.484","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX16 as ready","entity_name":"PEX16","entity_type":"gene"},{"created":"2025-12-24T16:06:09.741685+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.484","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex16 has been classified as Green List (High Evidence).","entity_name":"PEX16","entity_type":"gene"},{"created":"2025-12-24T16:06:07.515454+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.484","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX16 were changed from  to Peroxisome biogenesis disorder 8A (Zellweger) MIM#614876","entity_name":"PEX16","entity_type":"gene"},{"created":"2025-12-24T16:05:35.136523+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.483","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX16 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX16","entity_type":"gene"},{"created":"2025-12-24T16:05:04.856770+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.482","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX16: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 8A (Zellweger) MIM#614876; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX16","entity_type":"gene"},{"created":"2025-12-24T16:04:30.230587+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.482","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX14 as ready","entity_name":"PEX14","entity_type":"gene"},{"created":"2025-12-24T16:04:30.222964+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.482","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex14 has been classified as Green List (High Evidence).","entity_name":"PEX14","entity_type":"gene"},{"created":"2025-12-24T16:04:27.896442+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.482","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX14 were changed from  to Peroxisome biogenesis disorder 8A (Zellweger) MIM#614876","entity_name":"PEX14","entity_type":"gene"},{"created":"2025-12-24T16:04:02.445824+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.481","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX14","entity_type":"gene"},{"created":"2025-12-24T16:03:34.929292+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.480","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX14: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 8A (Zellweger) MIM#614876; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX14","entity_type":"gene"},{"created":"2025-12-24T16:02:59.162301+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.480","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX13 as ready","entity_name":"PEX13","entity_type":"gene"},{"created":"2025-12-24T16:02:59.154137+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.480","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex13 has been classified as Green List (High Evidence).","entity_name":"PEX13","entity_type":"gene"},{"created":"2025-12-24T16:02:56.734758+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.480","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX13 were changed from  to Peroxisome biogenesis disorder 11A (Zellweger) (MIM#614883)","entity_name":"PEX13","entity_type":"gene"},{"created":"2025-12-24T16:02:30.495480+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.479","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX13","entity_type":"gene"},{"created":"2025-12-24T16:02:03.987886+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.478","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX13: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 11A (Zellweger) (MIM#614883); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX13","entity_type":"gene"},{"created":"2025-12-24T15:35:45.229516+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.478","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX12 as ready","entity_name":"PEX12","entity_type":"gene"},{"created":"2025-12-24T15:35:45.218338+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.478","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex12 has been classified as Green List (High Evidence).","entity_name":"PEX12","entity_type":"gene"},{"created":"2025-12-24T15:35:43.042744+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.478","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX12 were changed from  to Peroxisome biogenesis disorder 3A (Zellweger) - MIM#614859","entity_name":"PEX12","entity_type":"gene"},{"created":"2025-12-24T15:35:17.569584+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.477","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX12","entity_type":"gene"},{"created":"2025-12-24T15:34:48.954519+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.476","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX12: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 3A (Zellweger) - MIM#614859; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX12","entity_type":"gene"},{"created":"2025-12-24T15:33:23.137903+11:00","panel_name":"Peroxisomal Disorders","panel_id":155,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX11B were set to 20301621; 22581968","entity_name":"PEX11B","entity_type":"gene"},{"created":"2025-12-24T15:32:49.710373+11:00","panel_name":"Peroxisomal Disorders","panel_id":155,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: PEX11B: Added comment: Additional families reported.; Changed publications: 20301621, 22581968, 38423277, 31724321, 28129423","entity_name":"PEX11B","entity_type":"gene"},{"created":"2025-12-24T15:32:23.255729+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3861","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX11B were set to 20301621; 22581968","entity_name":"PEX11B","entity_type":"gene"},{"created":"2025-12-24T15:32:02.688768+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3860","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: PEX11B: Added comment: Additional families reported.; Changed rating: GREEN; Changed publications: 38423277, 31724321, 28129423; Changed phenotypes: Peroxisome biogenesis disorder 14B - MIM#614920; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX11B","entity_type":"gene"},{"created":"2025-12-24T15:30:32.937155+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.476","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX11B as ready","entity_name":"PEX11B","entity_type":"gene"},{"created":"2025-12-24T15:30:32.927458+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.476","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex11b has been classified as Green List (High Evidence).","entity_name":"PEX11B","entity_type":"gene"},{"created":"2025-12-24T15:30:30.639637+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.476","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX11B were changed from  to Peroxisome biogenesis disorder 14B - MIM#614920","entity_name":"PEX11B","entity_type":"gene"},{"created":"2025-12-24T15:30:09.304478+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.475","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX11B were set to ","entity_name":"PEX11B","entity_type":"gene"},{"created":"2025-12-24T15:29:48.650773+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.474","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX11B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX11B","entity_type":"gene"},{"created":"2025-12-24T15:29:26.448822+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.473","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX11B: Rating: GREEN; Mode of pathogenicity: None; Publications: 38423277; Phenotypes: Peroxisome biogenesis disorder 14B - MIM#614920; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX11B","entity_type":"gene"},{"created":"2025-12-24T15:27:23.485937+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.473","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX10 as ready","entity_name":"PEX10","entity_type":"gene"},{"created":"2025-12-24T15:27:23.466250+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.473","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex10 has been classified as Green List (High Evidence).","entity_name":"PEX10","entity_type":"gene"},{"created":"2025-12-24T15:27:20.533358+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.473","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX10 were changed from  to Peroxisome biogenesis disorder 6A (Zellweger) MIM#614870","entity_name":"PEX10","entity_type":"gene"},{"created":"2025-12-24T15:26:57.799212+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.472","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX10","entity_type":"gene"},{"created":"2025-12-24T15:26:31.474076+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.471","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX10: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 6A (Zellweger) MIM#614870; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX10","entity_type":"gene"},{"created":"2025-12-24T15:25:41.398657+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.471","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX1 as ready","entity_name":"PEX1","entity_type":"gene"},{"created":"2025-12-24T15:25:41.391271+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.471","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex1 has been classified as Green List (High Evidence).","entity_name":"PEX1","entity_type":"gene"},{"created":"2025-12-24T15:25:39.308142+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.471","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX1 were changed from  to Peroxisome biogenesis disorder 1A (Zellweger) (MIM#214100)","entity_name":"PEX1","entity_type":"gene"},{"created":"2025-12-24T15:25:10.098952+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.470","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX1","entity_type":"gene"},{"created":"2025-12-24T15:24:42.674670+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.469","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 1A (Zellweger) (MIM#214100); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX1","entity_type":"gene"},{"created":"2025-12-24T15:22:48.047832+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3860","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PAX6 were changed from Coloboma of optic nerve - MIM# 120430; Coloboma, ocular - MIM#120200; Morning glory disc anomaly - MIM#120430; Aniridia - MIM#106210; Anterior segment dysgenesis 5, multiple subtypes - MIM#604229; Cataract with late-onset corneal dystrophy - MIM#106210; Foveal hypoplasia 1- MIM#136520; Keratitis - MIM#148190; Optic nerve hypoplasia - MIM#165550 to PAX6-related ocular dysgenesis MONDO:0800183","entity_name":"PAX6","entity_type":"gene"},{"created":"2025-12-24T15:22:23.549594+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3859","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PAX6: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: PAX6-related ocular dysgenesis MONDO:0800183; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PAX6","entity_type":"gene"},{"created":"2025-12-24T15:20:12.624334+11:00","panel_name":"Eye Anterior Segment Abnormalities","panel_id":43,"panel_version":"1.18","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PAX6 were changed from Aniridia MIM# 106210; Anterior segment dysgenesis 5, multiple subtypes MIM# 6042293; Cataract with late-onset corneal dystrophy MIM# 106210; Foveal hypoplasia 1 MIM# 136520; Keratitis MIM# 148190; Optic nerve hypoplasia MIM# 165550 to PAX6-related ocular dysgenesis MONDO:0800183","entity_name":"PAX6","entity_type":"gene"},{"created":"2025-12-24T15:19:40.065398+11:00","panel_name":"Eye Anterior Segment Abnormalities","panel_id":43,"panel_version":"1.17","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PAX6: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: PAX6-related ocular dysgenesis MONDO:0800183; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PAX6","entity_type":"gene"}]}