{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=934","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=932","results":[{"created":"2022-03-17T08:22:42.893736+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11480","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":"2022-03-17T08:19:39.447592+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11479","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IL1RN were set to ","entity_name":"IL1RN","entity_type":"gene"},{"created":"2022-03-17T08:19:16.995776+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11478","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":"2022-03-17T08:18:57.862848+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11477","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":"2022-03-16T20:48:00.716896+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11477","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IREB2 as ready","entity_name":"IREB2","entity_type":"gene"},{"created":"2022-03-16T20:48:00.706344+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11477","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ireb2 has been classified as Green List (High Evidence).","entity_name":"IREB2","entity_type":"gene"},{"created":"2022-03-16T20:47:46.337140+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11477","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IREB2 were changed from  to Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia, MIM#618451","entity_name":"IREB2","entity_type":"gene"},{"created":"2022-03-16T20:47:20.860740+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11476","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IREB2 were set to ","entity_name":"IREB2","entity_type":"gene"},{"created":"2022-03-16T20:46:59.787761+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11475","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IREB2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IREB2","entity_type":"gene"},{"created":"2022-03-16T20:45:47.723356+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ISG15 as ready","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:45:47.705089+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: isg15 has been classified as Green List (High Evidence).","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:45:45.110049+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ISG15 were changed from  to Immunodeficiency 38, MIM# 616126","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:45:16.797378+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ISG15 were set to ","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:44:46.526601+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ISG15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:44:13.465707+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ISG15: Rating: GREEN; Mode of pathogenicity: None; Publications: 25307056, 22859821, 35258551, 32944031; Phenotypes: Immunodeficiency 38, MIM# 616126; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:40:08.757653+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11474","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ISG15 as ready","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:40:08.747121+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11474","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: isg15 has been classified as Green List (High Evidence).","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:40:00.201162+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11474","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ISG15 were changed from  to Immunodeficiency 38, MIM# 616126","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:39:13.858426+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11473","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ISG15 were set to ","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:38:39.983702+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11472","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ISG15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:38:19.911130+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11471","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ISG15: Rating: GREEN; Mode of pathogenicity: None; Publications: 25307056, 22859821, 35258551, 32944031; Phenotypes: Immunodeficiency 38, MIM# 616126; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ISG15","entity_type":"gene"},{"created":"2022-03-16T20:35:52.796343+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11471","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ISCU as ready","entity_name":"ISCU","entity_type":"gene"},{"created":"2022-03-16T20:35:52.786803+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11471","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: iscu has been classified as Green List (High Evidence).","entity_name":"ISCU","entity_type":"gene"},{"created":"2022-03-16T20:35:44.153893+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11471","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ISCU were changed from  to Myopathy with lactic acidosis, hereditary, MIM# 255125","entity_name":"ISCU","entity_type":"gene"},{"created":"2022-03-16T20:35:24.601038+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11470","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ISCU were set to ","entity_name":"ISCU","entity_type":"gene"},{"created":"2022-03-16T20:35:02.659689+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11469","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ISCU was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ISCU","entity_type":"gene"},{"created":"2022-03-16T20:34:42.420396+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11468","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deep intronic tag was added to gene: ISCU.\nTag founder tag was added to gene: ISCU.","entity_name":"ISCU","entity_type":"gene"},{"created":"2022-03-16T20:34:28.497055+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11468","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ISCU: Rating: GREEN; Mode of pathogenicity: None; Publications: 29079705, 18304497, 18296749, 19567699; Phenotypes: Myopathy with lactic acidosis, hereditary, MIM# 255125; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ISCU","entity_type":"gene"},{"created":"2022-03-16T20:32:54.335377+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11468","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IRS1 as ready","entity_name":"IRS1","entity_type":"gene"},{"created":"2022-03-16T20:32:54.324344+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11468","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irs1 has been classified as Red List (Low Evidence).","entity_name":"IRS1","entity_type":"gene"},{"created":"2022-03-16T20:31:01.428832+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11468","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IRS1 were changed from  to {Coronary artery disease, susceptibility to}; {Type 2 diabetes mellitus, susceptibility to}, MIM# 125853","entity_name":"IRS1","entity_type":"gene"},{"created":"2022-03-16T20:27:50.660394+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11467","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IRS1 as Red List (low evidence)","entity_name":"IRS1","entity_type":"gene"},{"created":"2022-03-16T20:27:50.641729+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11467","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irs1 has been classified as Red List (Low Evidence).","entity_name":"IRS1","entity_type":"gene"},{"created":"2022-03-16T20:27:29.867819+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11466","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IRS1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Coronary artery disease, susceptibility to}, {Type 2 diabetes mellitus, susceptibility to}, MIM# 125853; Mode of inheritance: None","entity_name":"IRS1","entity_type":"gene"},{"created":"2022-03-16T20:25:35.088997+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IRF8 as ready","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:25:35.067677+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irf8 has been classified as Green List (High Evidence).","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:25:31.845958+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IRF8 were changed from  to Immunodeficiency 32A, mycobacteriosis, autosomal dominant, MIM# 614893; Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive, MIM# 226990","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:25:02.033319+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IRF8 were set to ","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:24:29.490637+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IRF8 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:23:52.133809+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IRF8: Rating: GREEN; Mode of pathogenicity: None; Publications: 21524210, 27893462, 29128673, 28162909, 25122610; Phenotypes: Immunodeficiency 32A, mycobacteriosis, autosomal dominant, MIM# 614893, Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive, MIM# 226990; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:20:29.127470+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11466","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IRF8 as ready","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:20:29.116118+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11466","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irf8 has been classified as Green List (High Evidence).","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:20:21.196682+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11466","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IRF8 were changed from  to Immunodeficiency 32A, mycobacteriosis, autosomal dominant, MIM# 614893; Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive, MIM# 226990","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:19:58.818901+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11465","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IRF8 were set to ","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:19:39.109254+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11464","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IRF8 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:19:19.812251+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11463","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IRF8: Rating: GREEN; Mode of pathogenicity: None; Publications: 21524210, 27893462, 29128673, 28162909, 25122610; Phenotypes: Immunodeficiency 32A, mycobacteriosis, autosomal dominant, MIM# 614893, Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive, MIM# 226990; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"IRF8","entity_type":"gene"},{"created":"2022-03-16T20:08:24.935779+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11463","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IRF5 as ready","entity_name":"IRF5","entity_type":"gene"},{"created":"2022-03-16T20:08:24.915755+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11463","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irf5 has been classified as Red List (Low Evidence).","entity_name":"IRF5","entity_type":"gene"},{"created":"2022-03-16T20:08:16.993610+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11463","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IRF5 were changed from  to {Inflammatory bowel disease 14} 612245; {Systemic lupus erythematosus, susceptibility to, 10} 612251","entity_name":"IRF5","entity_type":"gene"},{"created":"2022-03-16T20:07:55.709868+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11462","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IRF5 as Red List (low evidence)","entity_name":"IRF5","entity_type":"gene"},{"created":"2022-03-16T20:07:55.698917+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11462","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irf5 has been classified as Red List (Low Evidence).","entity_name":"IRF5","entity_type":"gene"},{"created":"2022-03-16T20:07:35.918982+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11461","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IRF5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: {Inflammatory bowel disease 14} 612245, {Systemic lupus erythematosus, susceptibility to, 10} 612251; Mode of inheritance: None","entity_name":"IRF5","entity_type":"gene"},{"created":"2022-03-16T20:06:05.038259+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11461","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IRF1 as ready","entity_name":"IRF1","entity_type":"gene"},{"created":"2022-03-16T20:06:05.019731+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11461","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irf1 has been classified as Red List (Low Evidence).","entity_name":"IRF1","entity_type":"gene"},{"created":"2022-03-16T20:05:56.482281+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11461","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IRF1 as Red List (low evidence)","entity_name":"IRF1","entity_type":"gene"},{"created":"2022-03-16T20:05:56.472817+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11461","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irf1 has been classified as Red List (Low Evidence).","entity_name":"IRF1","entity_type":"gene"},{"created":"2022-03-16T20:05:36.222336+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11460","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IRF1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"IRF1","entity_type":"gene"},{"created":"2022-03-16T20:04:37.872166+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.408","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IREB2 as ready","entity_name":"IREB2","entity_type":"gene"},{"created":"2022-03-16T20:04:37.853988+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.408","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ireb2 has been classified as Green List (High Evidence).","entity_name":"IREB2","entity_type":"gene"},{"created":"2022-03-16T20:04:25.498104+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.408","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IREB2 as Green List (high evidence)","entity_name":"IREB2","entity_type":"gene"},{"created":"2022-03-16T20:04:25.487459+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.408","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ireb2 has been classified as Green List (High Evidence).","entity_name":"IREB2","entity_type":"gene"},{"created":"2022-03-16T20:03:56.540291+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.407","user_name":"Zornitza Stark","item_type":"entity","text":"gene: IREB2 was added\ngene: IREB2 was added to Regression. Sources: Expert Review\nMode of inheritance for gene: IREB2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: IREB2 were set to 30915432; 31243445; 11175792\nPhenotypes for gene: IREB2 were set to Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia, MIM#618451\nReview for gene: IREB2 was set to GREEN\nAdded comment: Two affected individuals from unrelated families with functional evidence including concordant phenotype in mice. \nSources: Expert Review","entity_name":"IREB2","entity_type":"gene"},{"created":"2022-03-16T20:02:38.900744+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11460","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IREB2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30915432, 31243445, 11175792; Phenotypes: Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia, MIM#618451; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IREB2","entity_type":"gene"},{"created":"2022-03-16T19:59:49.567807+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.368","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA10 as ready","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:59:49.558988+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.368","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa10 has been classified as Red List (Low Evidence).","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:59:46.098033+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.368","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA10 were changed from  to Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:58:06.579368+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.367","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA10 were set to ","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:57:37.338944+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.366","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:57:09.403260+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.365","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA10 as Red List (low evidence)","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:57:09.393979+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.365","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa10 has been classified as Red List (Low Evidence).","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:56:37.829937+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.364","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA10: Rating: RED; Mode of pathogenicity: None; Publications: 21150889, 26741492, 28247337; Phenotypes: Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:53:51.605367+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.406","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA10 as ready","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:53:51.593993+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.406","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa10 has been classified as Green List (High Evidence).","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:53:46.515177+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.406","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA10 were changed from  to Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:53:16.760849+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.405","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA10 were set to ","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:52:18.741923+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.404","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:51:47.577698+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.403","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA10: Rating: GREEN; Mode of pathogenicity: None; Publications: 21150889, 26741492, 28247337; Phenotypes: Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:49:30.854742+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.715","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA10 as ready","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:49:30.832595+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.715","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa10 has been classified as Green List (High Evidence).","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:49:27.741788+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.715","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA10 were changed from Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243 to Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:48:53.302519+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.714","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA10 were changed from  to Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:48:13.065812+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.713","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA10 were set to ","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:47:34.614421+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.712","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:46:55.295542+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.711","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA10: Rating: GREEN; Mode of pathogenicity: None; Publications: 21150889, 26741492, 28247337; Phenotypes: Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:46:14.248667+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11460","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA10 were set to 26741492; 21150889","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T19:45:30.456656+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11459","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA10: Rating: GREEN; Mode of pathogenicity: None; Publications: 21150889, 26741492, 28247337; Phenotypes: Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:43:49.066198+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1487","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA10 as ready","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:43:49.054050+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1487","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa10 has been classified as Red List (Low Evidence).","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:41:29.110606+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1487","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA10 were changed from  to Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:40:54.263823+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1486","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA10 were set to ","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:40:14.609002+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1485","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:38:02.773886+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1484","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDUFA10 as Red List (low evidence)","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:38:02.751960+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1484","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa10 has been classified as Red List (Low Evidence).","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:37:24.664078+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1483","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDUFA10: Rating: RED; Mode of pathogenicity: None; Publications: 21150889, 26741492, 28247337; Phenotypes: Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:32:34.428778+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11459","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFA10 as ready","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:32:34.391093+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11459","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufa10 has been classified as Green List (High Evidence).","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:32:25.851500+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11459","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFA10 were changed from  to Mitochondrial complex I deficiency, nuclear type 22 - MIM#618243","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:32:05.154244+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11458","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFA10 were set to ","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:31:42.648560+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11457","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDUFA10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDUFA10","entity_type":"gene"},{"created":"2022-03-16T18:28:31.787142+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11456","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDST1 as ready","entity_name":"NDST1","entity_type":"gene"}]}