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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=834",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&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"
}
]
}