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{
"count": 220363,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=934",
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"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"
}
]
}