{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=834","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=832","results":[{"created":"2022-05-19T11:41:12.059137+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14516","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MITF were set to ","entity_name":"MITF","entity_type":"gene"},{"created":"2022-05-19T11:40:31.046967+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14515","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MITF was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MITF","entity_type":"gene"},{"created":"2022-05-19T11:40:00.924050+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14514","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MITF: Rating: GREEN; Mode of pathogenicity: None; Publications: 27889061, 32541011; Phenotypes: COMMAD syndrome, MIM# 617306, Tietz albinism-deafness syndrome, MIM# 103500, Waardenburg syndrome, type 2A, MIM# 193510; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"MITF","entity_type":"gene"},{"created":"2022-05-19T11:36:15.568127+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14514","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIR936 as ready","entity_name":"MIR936","entity_type":"gene"},{"created":"2022-05-19T11:36:15.539582+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14514","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir936 has been classified as Red List (Low Evidence).","entity_name":"MIR936","entity_type":"gene"},{"created":"2022-05-19T11:36:05.419479+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14514","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MIR936 as Red List (low evidence)","entity_name":"MIR936","entity_type":"gene"},{"created":"2022-05-19T11:36:05.407723+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14514","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir936 has been classified as Red List (Low Evidence).","entity_name":"MIR936","entity_type":"gene"},{"created":"2022-05-19T11:35:44.337813+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14513","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MIR936: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"MIR936","entity_type":"gene"},{"created":"2022-05-19T11:34:26.463575+10:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.339","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIR184 as ready","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:34:26.450555+10:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.339","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir184 has been classified as Green List (High Evidence).","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:34:23.991312+10:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.339","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MIR184 were changed from  to EDICT syndrome, MIM# 614303","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:33:53.034777+10:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.338","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MIR184 were set to ","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:33:20.588882+10:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.337","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MIR184 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:32:49.396801+10:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.336","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MIR184: Rating: GREEN; Mode of pathogenicity: None; Publications: 21996275, 22131394, 25373792, 24138095; Phenotypes: EDICT syndrome, MIM# 614303; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:32:22.511594+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14513","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIR184 as ready","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:32:22.499244+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14513","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir184 has been classified as Green List (High Evidence).","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:32:12.120375+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14513","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MIR184 were changed from  to EDICT syndrome, MIM# 614303","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:31:46.417117+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14512","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MIR184 were set to ","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:31:21.222308+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14511","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MIR184 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:30:57.241016+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14510","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MIR184: Rating: GREEN; Mode of pathogenicity: None; Publications: 21996275, 22131394, 25373792, 24138095; Phenotypes: EDICT syndrome, MIM# 614303; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MIR184","entity_type":"gene"},{"created":"2022-05-19T11:25:44.845630+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14510","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIR183 as ready","entity_name":"MIR183","entity_type":"gene"},{"created":"2022-05-19T11:25:44.834070+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14510","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir183 has been classified as Red List (Low Evidence).","entity_name":"MIR183","entity_type":"gene"},{"created":"2022-05-19T11:25:33.600275+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14510","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MIR183 as Red List (low evidence)","entity_name":"MIR183","entity_type":"gene"},{"created":"2022-05-19T11:25:33.584469+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14510","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir183 has been classified as Red List (Low Evidence).","entity_name":"MIR183","entity_type":"gene"},{"created":"2022-05-19T11:25:13.449117+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14509","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MIR183: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"MIR183","entity_type":"gene"},{"created":"2022-05-19T09:44:38.480222+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4787","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CPSF3 were changed from Neurodevelopmental disorder, CPSF3-related, MONDO:0700092 to Neurodevelopmental disorder with microcephaly, hypotonia, and seizures (NEDMHS), MIM#619876","entity_name":"CPSF3","entity_type":"gene"},{"created":"2022-05-19T09:43:59.303965+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4786","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CPSF3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder with microcephaly, hypotonia, and seizures (NEDMHS), MIM#619876; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CPSF3","entity_type":"gene"},{"created":"2022-05-19T09:39:57.645234+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1605","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CPSF3 were changed from Neurodevelopmental disorder, CPSF3-related, MONDO:0700092 to Neurodevelopmental disorder with microcephaly, hypotonia, and seizures (NEDMHS), MIM#619876","entity_name":"CPSF3","entity_type":"gene"},{"created":"2022-05-19T09:39:12.678512+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1604","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CPSF3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder with microcephaly, hypotonia, and seizures (NEDMHS), MIM#619876; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CPSF3","entity_type":"gene"},{"created":"2022-05-19T09:38:55.704804+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.123","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CPSF3 were changed from Neurodevelopmental disorder, CPSF3-related, MONDO:0700092 to Neurodevelopmental disorder with microcephaly, hypotonia, and seizures (NEDMHS), MIM#619876","entity_name":"CPSF3","entity_type":"gene"},{"created":"2022-05-19T09:38:19.359310+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.122","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CPSF3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder with microcephaly, hypotonia, and seizures (NEDMHS), MIM#619876; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CPSF3","entity_type":"gene"},{"created":"2022-05-19T09:37:55.018652+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14509","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CPSF3 were changed from Neurodevelopmental disorder, CPSF3-related, MONDO:0700092 to Neurodevelopmental disorder with microcephaly, hypotonia, and seizures (NEDMHS), MIM#619876","entity_name":"CPSF3","entity_type":"gene"},{"created":"2022-05-19T09:37:28.477395+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14508","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CPSF3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder with microcephaly, hypotonia, and seizures (NEDMHS), MIM#619876; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CPSF3","entity_type":"gene"},{"created":"2022-05-19T09:08:53.161424+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14508","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: ATP2C1 were set to 28551824","entity_name":"ATP2C1","entity_type":"gene"},{"created":"2022-05-19T09:08:47.243643+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14508","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ATP2C1 were changed from Hailey-Hailey disease (MIM# 169600) to Hailey-Hailey disease (MIM#169600)","entity_name":"ATP2C1","entity_type":"gene"},{"created":"2022-05-18T18:07:04.568561+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14507","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: ATP2C1 were changed from  to Hailey-Hailey disease (MIM# 169600)","entity_name":"ATP2C1","entity_type":"gene"},{"created":"2022-05-18T18:06:54.837984+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14506","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: ATP2C1 were set to ","entity_name":"ATP2C1","entity_type":"gene"},{"created":"2022-05-18T18:06:52.411527+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14506","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ATP2C1 as ready","entity_name":"ATP2C1","entity_type":"gene"},{"created":"2022-05-18T18:06:52.391973+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14506","user_name":"Elena Savva","item_type":"entity","text":"Gene: atp2c1 has been classified as Green List (High Evidence).","entity_name":"ATP2C1","entity_type":"gene"},{"created":"2022-05-18T18:06:48.850225+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14506","user_name":"Elena Savva","item_type":"entity","text":"Mode of inheritance for gene: ATP2C1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown","entity_name":"ATP2C1","entity_type":"gene"},{"created":"2022-05-18T18:06:22.825594+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14505","user_name":"Elena Savva","item_type":"entity","text":"Marked gene: ATP6V0A1 as ready","entity_name":"ATP6V0A1","entity_type":"gene"},{"created":"2022-05-18T18:06:22.814152+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14505","user_name":"Elena Savva","item_type":"entity","text":"Gene: atp6v0a1 has been classified as Green List (High Evidence).","entity_name":"ATP6V0A1","entity_type":"gene"},{"created":"2022-05-18T17:49:51.181059+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14505","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIR182 as ready","entity_name":"MIR182","entity_type":"gene"},{"created":"2022-05-18T17:49:51.168313+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14505","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir182 has been classified as Red List (Low Evidence).","entity_name":"MIR182","entity_type":"gene"},{"created":"2022-05-18T17:49:32.793857+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14505","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MIR182 as Red List (low evidence)","entity_name":"MIR182","entity_type":"gene"},{"created":"2022-05-18T17:49:32.784079+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14505","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mir182 has been classified as Red List (Low Evidence).","entity_name":"MIR182","entity_type":"gene"},{"created":"2022-05-18T17:47:51.011152+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14504","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MIR182: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"MIR182","entity_type":"gene"},{"created":"2022-05-18T17:46:24.697227+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14504","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIP as ready","entity_name":"MIP","entity_type":"gene"},{"created":"2022-05-18T17:46:24.685842+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14504","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mip has been classified as Green List (High Evidence).","entity_name":"MIP","entity_type":"gene"},{"created":"2022-05-18T17:46:08.922084+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14504","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MIP were changed from  to Cataract 15, multiple types, MIM# 615274","entity_name":"MIP","entity_type":"gene"},{"created":"2022-05-18T17:39:57.819498+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14503","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MIP were set to ","entity_name":"MIP","entity_type":"gene"},{"created":"2022-05-18T17:37:43.536218+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14502","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MIP was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MIP","entity_type":"gene"},{"created":"2022-05-18T17:37:05.221517+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14501","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MIP: Rating: GREEN; Mode of pathogenicity: None; Publications: 10802646, 16564824, 33530927, 30214549; Phenotypes: Cataract 15, multiple types, MIM# 615274; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MIP","entity_type":"gene"},{"created":"2022-05-18T17:28:47.607935+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14501","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MIF as ready","entity_name":"MIF","entity_type":"gene"},{"created":"2022-05-18T17:28:47.591375+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14501","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mif has been classified as Red List (Low Evidence).","entity_name":"MIF","entity_type":"gene"},{"created":"2022-05-18T17:28:32.538186+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14501","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MIF was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MIF","entity_type":"gene"},{"created":"2022-05-18T17:28:05.085608+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14500","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MIF were changed from  to {Rheumatoid arthritis, systemic juvenile, susceptibility to}, MIM# 604302","entity_name":"MIF","entity_type":"gene"},{"created":"2022-05-18T17:27:38.596329+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14499","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MIF as Red List (low evidence)","entity_name":"MIF","entity_type":"gene"},{"created":"2022-05-18T17:27:38.582122+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14499","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mif has been classified as Red List (Low Evidence).","entity_name":"MIF","entity_type":"gene"},{"created":"2022-05-18T17:27:12.507557+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14498","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MIF: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Rheumatoid arthritis, systemic juvenile, susceptibility to}, MIM# 604302; Mode of inheritance: None","entity_name":"MIF","entity_type":"gene"},{"created":"2022-05-18T17:25:08.887550+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.815","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MGME1 as ready","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:25:08.874756+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.815","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mgme1 has been classified as Green List (High Evidence).","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:25:05.660622+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.815","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MGME1 were changed from Mitochondrial DNA depletion syndrome 11, MIM# 615084 to Mitochondrial DNA depletion syndrome 11, MIM# 615084","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:24:31.109086+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.814","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MGME1 were changed from Mitochondrial DNA depletion syndrome 11, MIM# 615084 to Mitochondrial DNA depletion syndrome 11, MIM# 615084","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:21:53.096078+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.813","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MGME1 were changed from  to Mitochondrial DNA depletion syndrome 11, MIM# 615084","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:20:54.045678+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.812","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MGME1 were set to 23313956; 29572490; 28711739","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:20:25.489461+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.812","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MGME1 were set to ","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:19:55.317682+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.811","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MGME1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:19:25.059783+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.811","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MGME1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:19:02.475778+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14498","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MGME1 as ready","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:19:02.456710+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14498","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mgme1 has been classified as Green List (High Evidence).","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:18:40.075413+10:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.810","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MGME1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23313956, 29572490, 28711739; Phenotypes: Mitochondrial DNA depletion syndrome 11, MIM# 615084; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:18:39.047021+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14498","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MGME1 were changed from  to Mitochondrial DNA depletion syndrome 11, MIM# 615084","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:18:19.534978+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14497","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MGME1 were set to ","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:17:55.958394+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14496","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MGME1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:17:31.360950+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14495","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MGME1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23313956, 29572490, 28711739; Phenotypes: Mitochondrial DNA depletion syndrome 11, MIM# 615084; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MGME1","entity_type":"gene"},{"created":"2022-05-18T17:14:53.270141+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4786","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MFF as ready","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:14:53.252422+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4786","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mff has been classified as Green List (High Evidence).","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:13:23.951471+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14495","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MFN2 as ready","entity_name":"MFN2","entity_type":"gene"},{"created":"2022-05-18T17:13:23.938640+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14495","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mfn2 has been classified as Green List (High Evidence).","entity_name":"MFN2","entity_type":"gene"},{"created":"2022-05-18T17:13:09.058797+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14495","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MFN2 were set to ","entity_name":"MFN2","entity_type":"gene"},{"created":"2022-05-18T17:13:07.463881+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4786","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MFF were changed from  to Encephalopathy due to defective mitochondrial and peroxisomal fission 2, MIM# 617086","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:12:34.948053+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4785","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MFF were set to ","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:11:52.090716+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14494","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MFF as ready","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:11:52.077766+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14494","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mff has been classified as Green List (High Evidence).","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:11:43.193293+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4784","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MFF was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:11:03.610473+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4783","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MFF: Rating: GREEN; Mode of pathogenicity: None; Publications: 22499341, 26783368, 32181496; Phenotypes: Encephalopathy due to defective mitochondrial and peroxisomal fission 2, MIM# 617086; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:11:00.587383+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14494","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MFF were changed from  to Encephalopathy due to defective mitochondrial and peroxisomal fission 2, MIM# 617086","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:10:39.850357+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14493","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MFF were set to ","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:10:21.394975+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14492","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MFF was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:09:41.274676+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14491","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MFF: Rating: GREEN; Mode of pathogenicity: None; Publications: 22499341, 26783368, 32181496]; Phenotypes: Encephalopathy due to defective mitochondrial and peroxisomal fission 2, MIM# 617086; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MFF","entity_type":"gene"},{"created":"2022-05-18T17:07:00.692629+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14491","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: METTL23 as ready","entity_name":"METTL23","entity_type":"gene"},{"created":"2022-05-18T17:07:00.680536+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14491","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mettl23 has been classified as Green List (High Evidence).","entity_name":"METTL23","entity_type":"gene"},{"created":"2022-05-18T17:06:47.342747+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14491","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: METTL23 were changed from  to Intellectual developmental disorder, autosomal recessive 44, MIM# 615942","entity_name":"METTL23","entity_type":"gene"},{"created":"2022-05-18T17:06:19.839217+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14490","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: METTL23 were set to ","entity_name":"METTL23","entity_type":"gene"},{"created":"2022-05-18T17:05:54.467706+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14489","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: METTL23 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"METTL23","entity_type":"gene"},{"created":"2022-05-18T17:05:29.470870+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14488","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: METTL23: Rating: GREEN; Mode of pathogenicity: None; Publications: 24501276, 24626631; Phenotypes: Intellectual developmental disorder, autosomal recessive 44, MIM# 615942; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"METTL23","entity_type":"gene"},{"created":"2022-05-18T17:03:59.067127+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14488","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MET as ready","entity_name":"MET","entity_type":"gene"},{"created":"2022-05-18T17:03:59.053998+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14488","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: met has been classified as Green List (High Evidence).","entity_name":"MET","entity_type":"gene"},{"created":"2022-05-18T17:03:42.586023+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.14488","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MET were changed from  to Renal cell carcinoma, papillary, 1, familial and somatic, MIM# 605074; Papillary renal cell carcinoma MONDO:0017884","entity_name":"MET","entity_type":"gene"}]}