{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=933","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=931","results":[{"created":"2022-03-17T18:03:30.856337+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.416","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF1 as ready","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T18:03:30.845135+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.416","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf1 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T18:03:28.266886+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.416","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF1 were changed from  to Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T18:02:56.301449+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.415","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF1 were set to ","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:58:00.260670+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.414","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:57:28.903618+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.413","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFAF1 as Amber List (moderate evidence)","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:57:28.894768+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.413","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf1 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:56:58.591796+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.412","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFAF1: Rating: AMBER; Mode of pathogenicity: None; Publications: 17557076, 21931170, 16218961, 24963768, 34975718; Phenotypes: Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:55:37.763379+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.718","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF1 were changed from Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234 to Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:55:16.270449+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.718","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF1 as ready","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:55:16.259562+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.718","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf1 has been classified as Green List (High Evidence).","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:55:07.726409+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.718","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF1 were changed from  to Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:54:15.858177+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.717","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF1 were set to ","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:53:35.030565+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.716","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:52:56.815124+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.715","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFAF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17557076, 21931170, 16218961, 24963768, 34975718; Phenotypes: Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:51:53.872642+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11500","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF1 as ready","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:51:53.860835+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11500","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf1 has been classified as Green List (High Evidence).","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:51:46.194384+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11500","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF1 were changed from  to Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:51:26.272258+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11499","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF1 were set to ","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:50:56.924077+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11498","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFAF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T17:49:01.862520+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.372","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA9 as ready","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:49:01.843503+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.372","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa9 has been classified as Red List (Low Evidence).","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:48:58.441649+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.372","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA9 were changed from  to Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:48:23.999732+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.371","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA9 were set to ","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:47:53.415517+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.370","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:47:24.843922+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.369","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA9 as Red List (low evidence)","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:47:24.831397+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.369","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa9 has been classified as Red List (Low Evidence).","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:46:55.717235+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.368","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA9: Rating: RED; Mode of pathogenicity: None; Publications: 26425749, 28671271, 22114105; Phenotypes: Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:46:05.829376+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.412","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA9 as ready","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:46:05.816997+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.412","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa9 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:46:02.410417+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.412","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA9 were changed from  to Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:45:34.072796+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.411","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA9 were set to ","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:45:04.276848+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.410","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:44:36.944603+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.409","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA9 as Amber List (moderate evidence)","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:44:36.931275+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.409","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa9 has been classified as Amber List (Moderate Evidence).","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:44:07.294935+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.408","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA9: Rating: AMBER; Mode of pathogenicity: None; Publications: 26425749, 28671271, 22114105; Phenotypes: Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:42:35.820512+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11497","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA9 as ready","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:42:35.807042+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11497","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa9 has been classified as Green List (High Evidence).","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:42:27.976787+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11497","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA9 were changed from  to Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:42:08.597422+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11496","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA9 were set to ","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:41:46.252894+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11495","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T17:40:47.061024+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11494","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA7 as ready","entity_name":"NDUFA7","entity_type":"gene"},{"created":"2022-03-17T17:40:47.048074+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11494","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa7 has been classified as Red List (Low Evidence).","entity_name":"NDUFA7","entity_type":"gene"},{"created":"2022-03-17T17:39:23.127160+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11494","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA7 as Red List (low evidence)","entity_name":"NDUFA7","entity_type":"gene"},{"created":"2022-03-17T17:39:23.108211+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11494","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa7 has been classified as Red List (Low Evidence).","entity_name":"NDUFA7","entity_type":"gene"},{"created":"2022-03-17T17:38:45.751189+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11493","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TPTE2P5 as ready","entity_name":"TPTE2P5","entity_type":"gene"},{"created":"2022-03-17T17:38:45.740043+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11493","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tpte2p5 has been classified as Red List (Low Evidence).","entity_name":"TPTE2P5","entity_type":"gene"},{"created":"2022-03-17T17:38:11.553866+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11493","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TPTE2P5 as Red List (low evidence)","entity_name":"TPTE2P5","entity_type":"gene"},{"created":"2022-03-17T17:38:11.542936+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11493","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tpte2p5 has been classified as Red List (Low Evidence).","entity_name":"TPTE2P5","entity_type":"gene"},{"created":"2022-03-17T17:00:37.127999+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11492","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL6 as ready","entity_name":"IL6","entity_type":"gene"},{"created":"2022-03-17T17:00:37.118466+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11492","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il6 has been classified as Red List (Low Evidence).","entity_name":"IL6","entity_type":"gene"},{"created":"2022-03-17T17:00:27.006052+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11492","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL6 were changed from  to {Crohn disease-associated growth failure} 266600; {Intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to} 108010; {Rheumatoid arthritis, systemic juvenile} 604302; {Kaposi sarcoma, susceptibility to} 148000; {Type 1 diabetes mellitus} 222100; {Type 2 diabetes mellitus} 125853","entity_name":"IL6","entity_type":"gene"},{"created":"2022-03-17T17:00:04.607269+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11491","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IL6 as Red List (low evidence)","entity_name":"IL6","entity_type":"gene"},{"created":"2022-03-17T17:00:04.548462+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11491","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il6 has been classified as Red List (Low Evidence).","entity_name":"IL6","entity_type":"gene"},{"created":"2022-03-17T16:59:45.278589+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11490","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: IL6: Changed rating: RED","entity_name":"IL6","entity_type":"gene"},{"created":"2022-03-17T16:59:35.996282+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11490","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL6: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: {Crohn disease-associated growth failure} 266600, {Intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to} 108010, {Rheumatoid arthritis, systemic juvenile} 604302, {Kaposi sarcoma, susceptibility to} 148000, {Type 1 diabetes mellitus} 222100, {Type 2 diabetes mellitus} 125853; Mode of inheritance: None","entity_name":"IL6","entity_type":"gene"},{"created":"2022-03-17T16:55:07.069828+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11490","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL4 as ready","entity_name":"IL4","entity_type":"gene"},{"created":"2022-03-17T16:55:07.060038+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11490","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il4 has been classified as Red List (Low Evidence).","entity_name":"IL4","entity_type":"gene"},{"created":"2022-03-17T16:54:58.267148+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11490","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IL4 as Red List (low evidence)","entity_name":"IL4","entity_type":"gene"},{"created":"2022-03-17T16:54:58.255256+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11490","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il4 has been classified as Red List (Low Evidence).","entity_name":"IL4","entity_type":"gene"},{"created":"2022-03-17T16:54:39.371249+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11489","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"IL4","entity_type":"gene"},{"created":"2022-03-17T16:53:48.469102+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11489","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL36RN as ready","entity_name":"IL36RN","entity_type":"gene"},{"created":"2022-03-17T16:53:48.459340+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11489","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il36rn has been classified as Green List (High Evidence).","entity_name":"IL36RN","entity_type":"gene"},{"created":"2022-03-17T16:53:40.254087+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11489","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL36RN were changed from  to Psoriasis 14, pustular, MIM# 614204","entity_name":"IL36RN","entity_type":"gene"},{"created":"2022-03-17T16:53:14.670906+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11488","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IL36RN were set to ","entity_name":"IL36RN","entity_type":"gene"},{"created":"2022-03-17T16:52:51.624421+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11487","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IL36RN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IL36RN","entity_type":"gene"},{"created":"2022-03-17T16:52:29.999742+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11486","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL36RN: Rating: GREEN; Mode of pathogenicity: None; Publications: 21848462, 21839423, 22903787, 23648549; Phenotypes: Psoriasis 14, pustular, MIM# 614204; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IL36RN","entity_type":"gene"},{"created":"2022-03-17T16:48:51.986159+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL31RA as ready","entity_name":"IL31RA","entity_type":"gene"},{"created":"2022-03-17T16:48:51.975757+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11486","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il31ra has been classified as Red List (Low Evidence).","entity_name":"IL31RA","entity_type":"gene"},{"created":"2022-03-17T16:48:01.400913+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11486","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL31RA were changed from  to Amyloidosis, primary localized cutaneous, 2, MIM# 613955","entity_name":"IL31RA","entity_type":"gene"},{"created":"2022-03-17T16:47:36.265533+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11485","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IL31RA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"IL31RA","entity_type":"gene"},{"created":"2022-03-17T16:47:17.084741+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11484","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IL31RA as Red List (low evidence)","entity_name":"IL31RA","entity_type":"gene"},{"created":"2022-03-17T16:47:17.059611+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11484","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il31ra has been classified as Red List (Low Evidence).","entity_name":"IL31RA","entity_type":"gene"},{"created":"2022-03-17T16:46:52.572230+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11483","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL31RA: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Amyloidosis, primary localized cutaneous, 2, MIM#  613955; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"IL31RA","entity_type":"gene"},{"created":"2022-03-17T11:31:16.540429+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.408","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T11:31:03.246778+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1487","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T11:30:54.843979+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.715","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T11:30:34.567153+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11483","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: 33528536, 34364746, 16200211, 19384974, 20571988; Phenotypes: Mitochondrial complex I deficiency, nuclear type 10 - MIM#618233; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2022-03-17T11:27:54.018447+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.408","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFAF1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T11:27:19.577976+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.715","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFAF1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T11:27:06.721120+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11483","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFAF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17557076, 21931170, 16218961, 24963768, 34975718; Phenotypes: Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFAF1","entity_type":"gene"},{"created":"2022-03-17T11:13:22.423036+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.368","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFA9: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T11:12:53.146322+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.408","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFA9: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T11:11:45.386312+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11483","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFA9: Rating: GREEN; Mode of pathogenicity: None; Publications: 26425749, 28671271, 22114105; Phenotypes: Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA9","entity_type":"gene"},{"created":"2022-03-17T10:50:54.396975+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11483","user_name":"Krithika Murali","item_type":"entity","text":"reviewed gene: NDUFA7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"NDUFA7","entity_type":"gene"},{"created":"2022-03-17T10:26:04.053068+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11483","user_name":"Michelle Torres","item_type":"entity","text":"reviewed gene: TPTE2P5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TPTE2P5","entity_type":"gene"},{"created":"2022-03-17T08:46:33.377757+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11483","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL2RA as ready","entity_name":"IL2RA","entity_type":"gene"},{"created":"2022-03-17T08:46:33.363677+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11483","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il2ra has been classified as Green List (High Evidence).","entity_name":"IL2RA","entity_type":"gene"},{"created":"2022-03-17T08:46:23.970460+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11483","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL2RA were changed from  to Immunodeficiency 41 with lymphoproliferation and autoimmunity, MIM# 606367","entity_name":"IL2RA","entity_type":"gene"},{"created":"2022-03-17T08:46:01.078902+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11482","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IL2RA were set to ","entity_name":"IL2RA","entity_type":"gene"},{"created":"2022-03-17T08:45:38.096178+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11481","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IL2RA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IL2RA","entity_type":"gene"},{"created":"2022-03-17T08:45:16.175997+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11480","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL2RA: Rating: GREEN; Mode of pathogenicity: None; Publications: 9096364, 17196245, 23416241, 24116927; Phenotypes: Immunodeficiency 41 with lymphoproliferation and autoimmunity, MIM# 606367; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IL2RA","entity_type":"gene"},{"created":"2022-03-17T08:27:53.035749+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL1RN as ready","entity_name":"IL1RN","entity_type":"gene"},{"created":"2022-03-17T08:27:53.023518+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il1rn has been classified as Green List (High Evidence).","entity_name":"IL1RN","entity_type":"gene"},{"created":"2022-03-17T08:27:50.575770+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL1RN were changed from  to Interleukin 1 receptor antagonist deficiency, MIM# 612852","entity_name":"IL1RN","entity_type":"gene"},{"created":"2022-03-17T08:24:44.854565+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IL1RN were set to ","entity_name":"IL1RN","entity_type":"gene"},{"created":"2022-03-17T08:24:14.165735+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IL1RN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IL1RN","entity_type":"gene"},{"created":"2022-03-17T08:23:41.671483+11:00","panel_name":"Systemic Autoinflammatory Disease_Periodic Fever","panel_id":238,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL1RN: Rating: GREEN; Mode of pathogenicity: None; Publications: 19494218, 32819369; Phenotypes: Interleukin 1 receptor antagonist deficiency, MIM# 612852; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IL1RN","entity_type":"gene"},{"created":"2022-03-17T08:22:54.232915+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11480","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL1RN as ready","entity_name":"IL1RN","entity_type":"gene"},{"created":"2022-03-17T08:22:54.220867+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11480","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il1rn has been classified as Green List (High Evidence).","entity_name":"IL1RN","entity_type":"gene"}]}