{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=835","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=833","results":[{"created":"2022-05-18T17:03:17.719407+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14487","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MET was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MET","entity_type":"gene"},{"created":"2022-05-18T17:02:55.680304+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14486","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: MET: Changed phenotypes: Renal cell carcinoma, papillary, 1, familial and somatic, MIM# 605074, Papillary renal cell carcinoma MONDO:0017884","entity_name":"MET","entity_type":"gene"},{"created":"2022-05-18T17:02:31.900346+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14486","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MET: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Papillary renal cell carcinoma MONDO:0017884; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MET","entity_type":"gene"},{"created":"2022-05-18T16:59:39.532991+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MERTK as ready","entity_name":"MERTK","entity_type":"gene"},{"created":"2022-05-18T16:59:39.518965+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mertk has been classified as Green List (High Evidence).","entity_name":"MERTK","entity_type":"gene"},{"created":"2022-05-18T16:59:34.142305+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MERTK were changed from childhood onset rod-cone dystrophy with early macular atrophy; Leber congenital amaurosisRetinitis pigmentosa 38, 613862 to Retinitis pigmentosa 38, MIM# 613862","entity_name":"MERTK","entity_type":"gene"},{"created":"2022-05-18T16:59:20.644198+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MERTK were set to ","entity_name":"MERTK","entity_type":"gene"},{"created":"2022-05-18T16:58:39.756335+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14486","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ATG16L1 as ready","entity_name":"ATG16L1","entity_type":"gene"},{"created":"2022-05-18T16:58:39.746730+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14486","user_name":"Elena Savva","item_type":"entity","text":"Gene: atg16l1 has been classified as Red List (Low Evidence).","entity_name":"ATG16L1","entity_type":"gene"},{"created":"2022-05-18T16:56:53.607980+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MERTK: Rating: GREEN; Mode of pathogenicity: None; Publications: 11062461, 17301963, 20300561, 22180149; Phenotypes: Retinitis pigmentosa 38, MIM# 613862; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MERTK","entity_type":"gene"},{"created":"2022-05-18T16:56:05.748955+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MERTK as ready","entity_name":"MERTK","entity_type":"gene"},{"created":"2022-05-18T16:56:05.736185+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14486","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mertk has been classified as Green List (High Evidence).","entity_name":"MERTK","entity_type":"gene"},{"created":"2022-05-18T16:55:54.205867+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14486","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MERTK were changed from  to Retinitis pigmentosa 38, MIM# 613862","entity_name":"MERTK","entity_type":"gene"},{"created":"2022-05-18T16:55:28.025331+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14485","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MERTK were set to ","entity_name":"MERTK","entity_type":"gene"},{"created":"2022-05-18T16:55:02.261288+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14484","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MERTK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MERTK","entity_type":"gene"},{"created":"2022-05-18T16:54:37.430555+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14483","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MERTK: Rating: GREEN; Mode of pathogenicity: None; Publications: 11062461, 17301963, 20300561, 22180149; Phenotypes: Retinitis pigmentosa 38, MIM# 613862; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MERTK","entity_type":"gene"},{"created":"2022-05-18T16:52:21.403693+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14483","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MEIS1 as ready","entity_name":"MEIS1","entity_type":"gene"},{"created":"2022-05-18T16:52:21.391727+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14483","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: meis1 has been classified as Red List (Low Evidence).","entity_name":"MEIS1","entity_type":"gene"},{"created":"2022-05-18T16:52:04.387110+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14483","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MEIS1 as Red List (low evidence)","entity_name":"MEIS1","entity_type":"gene"},{"created":"2022-05-18T16:52:04.369007+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14483","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: meis1 has been classified as Red List (Low Evidence).","entity_name":"MEIS1","entity_type":"gene"},{"created":"2022-05-18T16:51:17.811123+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14482","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MEIS1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"MEIS1","entity_type":"gene"},{"created":"2022-05-18T16:44:57.098142+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14482","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ATP1A1 were changed from Charcot-Marie-Tooth disease, axonal, type 2DD MIM#618036; Hypomagnesemia, seizures, and mental retardation 2 MIM#618314 to Charcot-Marie-Tooth disease, axonal, type 2DD MIM#618036; Hypomagnesemia, seizures, and mental retardation 2 MIM#618314","entity_name":"ATP1A1","entity_type":"gene"},{"created":"2022-05-18T16:42:45.936742+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14481","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ATP2A2 as ready","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2022-05-18T16:42:45.926360+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14481","user_name":"Elena Savva","item_type":"entity","text":"Gene: atp2a2 has been classified as Green List (High Evidence).","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2022-05-18T16:41:09.286093+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14481","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ATG16L1 were changed from  to {Inflammatory bowel disease (Crohn disease) 10} MIM#611081","entity_name":"ATG16L1","entity_type":"gene"},{"created":"2022-05-18T16:40:58.689666+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14480","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: ATG16L1 were set to ","entity_name":"ATG16L1","entity_type":"gene"},{"created":"2022-05-18T16:40:50.475923+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14480","user_name":"Elena Savva","item_type":"entity","text":"Classified gene: ATG16L1 as Red List (low evidence)","entity_name":"ATG16L1","entity_type":"gene"},{"created":"2022-05-18T16:40:50.452506+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14480","user_name":"Elena Savva","item_type":"entity","text":"Gene: atg16l1 has been classified as Red List (Low Evidence).","entity_name":"ATG16L1","entity_type":"gene"},{"created":"2022-05-18T16:34:39.171235+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14479","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ATL3 were changed from Neuropathy, hereditary sensory, type IF, MIM# 615632 to Neuropathy, hereditary sensory, type IF, MIM# 615632","entity_name":"ATL3","entity_type":"gene"},{"created":"2022-05-18T16:34:02.254313+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14478","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ATP2A2 were changed from  to Acrokeratosis verruciformis MIM#101900; Darier disease MIM#124200","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2022-05-18T16:33:57.871818+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14477","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: ATP2A2 were set to ","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2022-05-18T16:33:51.547032+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14477","user_name":"Elena Savva","item_type":"entity","text":"Mode of inheritance for gene: ATP2A2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2022-05-18T16:31:23.888158+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14476","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ATP1A1 were changed from  to Charcot-Marie-Tooth disease, axonal, type 2DD MIM#618036; Hypomagnesemia, seizures, and mental retardation 2 MIM#618314","entity_name":"ATP1A1","entity_type":"gene"},{"created":"2022-05-18T16:31:10.827100+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14475","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ATP1A1 as ready","entity_name":"ATP1A1","entity_type":"gene"},{"created":"2022-05-18T16:31:10.811952+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14475","user_name":"Elena Savva","item_type":"entity","text":"Gene: atp1a1 has been classified as Green List (High Evidence).","entity_name":"ATP1A1","entity_type":"gene"},{"created":"2022-05-18T16:29:02.678226+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14475","user_name":"Elena Savva","item_type":"entity","text":"reviewed gene: ATG16L1: Rating: ; Mode of pathogenicity: None; Publications: PMID: 20602997; Phenotypes: {Inflammatory bowel disease (Crohn disease) 10} MIM#611081; Mode of inheritance: None","entity_name":"ATG16L1","entity_type":"gene"},{"created":"2022-05-18T16:27:26.549963+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14475","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ATL3 were changed from  to Neuropathy, hereditary sensory, type IF, MIM# 615632","entity_name":"ATL3","entity_type":"gene"},{"created":"2022-05-18T16:27:25.363081+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14474","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ATL3 as ready","entity_name":"ATL3","entity_type":"gene"},{"created":"2022-05-18T16:27:25.350098+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14474","user_name":"Elena Savva","item_type":"entity","text":"Gene: atl3 has been classified as Green List (High Evidence).","entity_name":"ATL3","entity_type":"gene"},{"created":"2022-05-18T16:27:10.422854+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14474","user_name":"Elena Savva","item_type":"entity","text":"reviewed gene: ATP2A2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 24336169; Phenotypes: Acrokeratosis verruciformis MIM#101900, Darier disease MIM#124200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2022-05-18T16:24:12.988192+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14474","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: ATP1A1 were set to ","entity_name":"ATP1A1","entity_type":"gene"},{"created":"2022-05-18T16:24:04.972066+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14474","user_name":"Elena Savva","item_type":"entity","text":"Mode of inheritance for gene: ATP1A1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","entity_name":"ATP1A1","entity_type":"gene"},{"created":"2022-05-18T16:21:59.254916+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14473","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: ATL3 were set to ","entity_name":"ATL3","entity_type":"gene"},{"created":"2022-05-18T16:21:46.944394+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14473","user_name":"Elena Savva","item_type":"entity","text":"Mode of inheritance for gene: ATL3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","entity_name":"ATL3","entity_type":"gene"},{"created":"2022-05-18T16:09:00.152042+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14472","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ATF1 as ready","entity_name":"ATF1","entity_type":"gene"},{"created":"2022-05-18T16:09:00.134022+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14472","user_name":"Elena Savva","item_type":"entity","text":"Gene: atf1 has been classified as Red List (Low Evidence).","entity_name":"ATF1","entity_type":"gene"},{"created":"2022-05-18T16:00:58.014416+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14472","user_name":"Elena Savva","item_type":"entity","text":"Classified gene: ATF1 as Red List (low evidence)","entity_name":"ATF1","entity_type":"gene"},{"created":"2022-05-18T16:00:58.001756+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14472","user_name":"Elena Savva","item_type":"entity","text":"Gene: atf1 has been classified as Red List (Low Evidence).","entity_name":"ATF1","entity_type":"gene"},{"created":"2022-05-18T16:00:53.944473+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14471","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MEIOB as ready","entity_name":"MEIOB","entity_type":"gene"},{"created":"2022-05-18T16:00:53.928680+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14471","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: meiob has been classified as Green List (High Evidence).","entity_name":"MEIOB","entity_type":"gene"},{"created":"2022-05-18T16:00:37.881341+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14471","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ASPN as ready","entity_name":"ASPN","entity_type":"gene"},{"created":"2022-05-18T16:00:37.868860+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14471","user_name":"Elena Savva","item_type":"entity","text":"Gene: aspn has been classified as Red List (Low Evidence).","entity_name":"ASPN","entity_type":"gene"},{"created":"2022-05-18T16:00:11.897592+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14471","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MEGF8 as ready","entity_name":"MEGF8","entity_type":"gene"},{"created":"2022-05-18T16:00:11.885720+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14471","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: megf8 has been classified as Green List (High Evidence).","entity_name":"MEGF8","entity_type":"gene"},{"created":"2022-05-18T16:00:01.108956+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14471","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MEGF8 were changed from  to Carpenter syndrome, MIM#614976","entity_name":"MEGF8","entity_type":"gene"},{"created":"2022-05-18T15:59:36.632101+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14470","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MEGF8 were set to ","entity_name":"MEGF8","entity_type":"gene"},{"created":"2022-05-18T15:59:12.896019+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14469","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MEGF8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MEGF8","entity_type":"gene"},{"created":"2022-05-18T15:58:50.920536+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14468","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MEGF8: Rating: GREEN; Mode of pathogenicity: None; Publications: 23063620; Phenotypes: Carpenter syndrome, MIM#614976; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MEGF8","entity_type":"gene"},{"created":"2022-05-18T15:56:01.390964+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14468","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MEFV as ready","entity_name":"MEFV","entity_type":"gene"},{"created":"2022-05-18T15:56:01.374543+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14468","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mefv has been classified as Green List (High Evidence).","entity_name":"MEFV","entity_type":"gene"},{"created":"2022-05-18T15:55:50.576875+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14468","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: ASPN were set to ","entity_name":"ASPN","entity_type":"gene"},{"created":"2022-05-18T15:55:35.062376+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14467","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MEFV were changed from  to Familial Mediterranean fever MIM# 249100","entity_name":"MEFV","entity_type":"gene"},{"created":"2022-05-18T15:55:09.890875+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14466","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MEFV was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MEFV","entity_type":"gene"},{"created":"2022-05-18T15:54:47.464646+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14465","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MEFV: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Familial Mediterranean fever MIM# 249100; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MEFV","entity_type":"gene"},{"created":"2022-05-18T15:53:16.390177+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14465","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MED23 as ready","entity_name":"MED23","entity_type":"gene"},{"created":"2022-05-18T15:53:16.380138+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14465","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: med23 has been classified as Green List (High Evidence).","entity_name":"MED23","entity_type":"gene"},{"created":"2022-05-18T15:53:05.173358+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14465","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MED23 were changed from  to Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy, MIM# 614249","entity_name":"MED23","entity_type":"gene"},{"created":"2022-05-18T15:52:41.541040+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14464","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MED23 were set to ","entity_name":"MED23","entity_type":"gene"},{"created":"2022-05-18T15:52:18.284739+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14463","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MED23 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MED23","entity_type":"gene"},{"created":"2022-05-18T15:51:56.530724+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14462","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MED23: Rating: GREEN; Mode of pathogenicity: None; Publications: 21868677, 25845469, 27311965, 30847200, 31164858; Phenotypes: Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy, MIM# 614249; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MED23","entity_type":"gene"},{"created":"2022-05-18T15:49:16.203074+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14462","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MED13 as ready","entity_name":"MED13","entity_type":"gene"},{"created":"2022-05-18T15:49:16.188217+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14462","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: med13 has been classified as Green List (High Evidence).","entity_name":"MED13","entity_type":"gene"},{"created":"2022-05-18T15:49:06.129690+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14462","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MED13 were changed from  to Intellectual developmental disorder, autosomal dominant 61, MIM# 618009","entity_name":"MED13","entity_type":"gene"},{"created":"2022-05-18T15:48:41.406695+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14461","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MED13 were set to ","entity_name":"MED13","entity_type":"gene"},{"created":"2022-05-18T15:48:19.038845+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14460","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MED13 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MED13","entity_type":"gene"},{"created":"2022-05-18T15:47:56.440823+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14459","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MED13: Rating: GREEN; Mode of pathogenicity: None; Publications: 29740699; Phenotypes: Intellectual developmental disorder, autosomal dominant 61, MIM# 618009; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MED13","entity_type":"gene"},{"created":"2022-05-18T15:43:59.382774+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14459","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MECP2 as ready","entity_name":"MECP2","entity_type":"gene"},{"created":"2022-05-18T15:43:59.367112+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14459","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mecp2 has been classified as Green List (High Evidence).","entity_name":"MECP2","entity_type":"gene"},{"created":"2022-05-18T15:43:42.248238+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14459","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MECP2 were changed from  to Rett syndrome, MIM# 312750; Intellectual developmental disorder, X-linked, syndromic 13, MIM# 300055; Encephalopathy, neonatal severe, MIM# 300673","entity_name":"MECP2","entity_type":"gene"},{"created":"2022-05-18T15:43:18.080557+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14458","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MECP2 were set to ","entity_name":"MECP2","entity_type":"gene"},{"created":"2022-05-18T15:42:47.679710+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14457","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MECP2 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"MECP2","entity_type":"gene"},{"created":"2022-05-18T15:42:23.948957+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14456","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MECP2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Rett syndrome, MIM# 312750, Intellectual developmental disorder, X-linked, syndromic 13, MIM# 300055, Encephalopathy, neonatal severe, MIM# 300673; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"MECP2","entity_type":"gene"},{"created":"2022-05-18T15:40:40.574919+10:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.300","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MCM9 as ready","entity_name":"MCM9","entity_type":"gene"},{"created":"2022-05-18T15:40:40.562821+10:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.300","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcm9 has been classified as Green List (High Evidence).","entity_name":"MCM9","entity_type":"gene"},{"created":"2022-05-18T15:40:37.731472+10:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.300","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MCM9 were changed from Ovarian dysgenesis 4, 616185 to Ovarian dysgenesis 4, MIM#616185","entity_name":"MCM9","entity_type":"gene"},{"created":"2022-05-18T15:40:29.982719+10:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.299","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MCM9 were set to ","entity_name":"MCM9","entity_type":"gene"},{"created":"2022-05-18T15:40:17.718645+10:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.298","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MCM9: Rating: GREEN; Mode of pathogenicity: None; Publications: 25480036, 26771056, 33538981, 33095795; Phenotypes: Ovarian dysgenesis 4, MIM# 616185; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MCM9","entity_type":"gene"},{"created":"2022-05-18T15:39:25.325006+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14456","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MCM9 as ready","entity_name":"MCM9","entity_type":"gene"},{"created":"2022-05-18T15:39:25.312355+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14456","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcm9 has been classified as Green List (High Evidence).","entity_name":"MCM9","entity_type":"gene"},{"created":"2022-05-18T15:39:14.408006+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14456","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MCM9 were changed from  to Ovarian dysgenesis 4, MIM# 616185","entity_name":"MCM9","entity_type":"gene"},{"created":"2022-05-18T15:38:48.066953+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14455","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MCM9 were set to ","entity_name":"MCM9","entity_type":"gene"},{"created":"2022-05-18T15:38:16.352870+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14454","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MCM9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MCM9","entity_type":"gene"},{"created":"2022-05-18T15:37:54.122970+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14453","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MCM9: Rating: GREEN; Mode of pathogenicity: None; Publications: 25480036, 26771056, 33538981, 33095795; Phenotypes: Ovarian dysgenesis 4, MIM# 616185; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MCM9","entity_type":"gene"},{"created":"2022-05-18T15:34:47.497925+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14453","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MCM8 as ready","entity_name":"MCM8","entity_type":"gene"},{"created":"2022-05-18T15:34:47.475034+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14453","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcm8 has been classified as Green List (High Evidence).","entity_name":"MCM8","entity_type":"gene"},{"created":"2022-05-18T15:19:08.784652+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14453","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ASPN were changed from {Lumbar disc degeneration} MIM#603932; {Osteoarthritis susceptibility 3} MIM#607850 to {Lumbar disc degeneration} MIM#603932; {Osteoarthritis susceptibility 3} MIM#607850","entity_name":"ASPN","entity_type":"gene"},{"created":"2022-05-18T15:19:08.552111+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14453","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ASPN were changed from  to {Lumbar disc degeneration} MIM#603932; {Osteoarthritis susceptibility 3} MIM#607850","entity_name":"ASPN","entity_type":"gene"},{"created":"2022-05-18T15:17:35.355002+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14452","user_name":"Elena Savva","item_type":"entity","text":"Classified gene: ASPN as Red List (low evidence)","entity_name":"ASPN","entity_type":"gene"},{"created":"2022-05-18T15:17:35.341978+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14452","user_name":"Elena Savva","item_type":"entity","text":"Gene: aspn has been classified as Red List (Low Evidence).","entity_name":"ASPN","entity_type":"gene"},{"created":"2022-05-18T15:17:21.894361+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14451","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ARV1 as ready","entity_name":"ARV1","entity_type":"gene"}]}