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{
"count": 220363,
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{
"created": "2022-03-17T18:03:30.856337+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.416",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF1 as ready",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T18:03:30.845135+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.416",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T18:03:28.266886+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.416",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF1 were changed from to Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T18:02:56.301449+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.415",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFAF1 were set to ",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:58:00.260670+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.414",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFAF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:57:28.903618+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFAF1 as Amber List (moderate evidence)",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:57:28.894768+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.413",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:56:58.591796+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.412",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFAF1: Rating: AMBER; Mode of pathogenicity: None; Publications: 17557076, 21931170, 16218961, 24963768, 34975718; Phenotypes: Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:55:37.763379+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.718",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF1 were changed from Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234 to Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:55:16.270449+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.718",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF1 as ready",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:55:16.259562+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.718",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf1 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:55:07.726409+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.718",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF1 were changed from to Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:54:15.858177+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.717",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFAF1 were set to ",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:53:35.030565+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.716",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFAF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:52:56.815124+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.715",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFAF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17557076, 21931170, 16218961, 24963768, 34975718; Phenotypes: Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:51:53.872642+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11500",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFAF1 as ready",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:51:53.860835+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11500",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufaf1 has been classified as Green List (High Evidence).",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:51:46.194384+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11500",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFAF1 were changed from to Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:51:26.272258+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11499",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFAF1 were set to ",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:50:56.924077+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFAF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:49:01.862520+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFA9 as ready",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:49:01.843503+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufa9 has been classified as Red List (Low Evidence).",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:48:58.441649+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.372",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFA9 were changed from to Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:48:23.999732+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.371",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFA9 were set to ",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:47:53.415517+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.370",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFA9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:47:24.843922+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.369",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFA9 as Red List (low evidence)",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:47:24.831397+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.369",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufa9 has been classified as Red List (Low Evidence).",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:46:55.717235+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.368",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFA9: Rating: RED; Mode of pathogenicity: None; Publications: 26425749, 28671271, 22114105; Phenotypes: Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:46:05.829376+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.412",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFA9 as ready",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:46:05.816997+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.412",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufa9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:46:02.410417+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.412",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFA9 were changed from to Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:45:34.072796+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.411",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFA9 were set to ",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:45:04.276848+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.410",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFA9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:44:36.944603+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.409",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFA9 as Amber List (moderate evidence)",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:44:36.931275+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.409",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufa9 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:44:07.294935+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.408",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDUFA9: Rating: AMBER; Mode of pathogenicity: None; Publications: 26425749, 28671271, 22114105; Phenotypes: Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:42:35.820512+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11497",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFA9 as ready",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:42:35.807042+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11497",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufa9 has been classified as Green List (High Evidence).",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:42:27.976787+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11497",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFA9 were changed from to Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:42:08.597422+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFA9 were set to ",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:41:46.252894+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11495",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDUFA9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:40:47.061024+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFA7 as ready",
"entity_name": "NDUFA7",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:40:47.048074+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufa7 has been classified as Red List (Low Evidence).",
"entity_name": "NDUFA7",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:39:23.127160+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDUFA7 as Red List (low evidence)",
"entity_name": "NDUFA7",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:39:23.108211+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufa7 has been classified as Red List (Low Evidence).",
"entity_name": "NDUFA7",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:38:45.751189+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TPTE2P5 as ready",
"entity_name": "TPTE2P5",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:38:45.740043+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tpte2p5 has been classified as Red List (Low Evidence).",
"entity_name": "TPTE2P5",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:38:11.553866+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TPTE2P5 as Red List (low evidence)",
"entity_name": "TPTE2P5",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:38:11.542936+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tpte2p5 has been classified as Red List (Low Evidence).",
"entity_name": "TPTE2P5",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:00:37.127999+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11492",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL6 as ready",
"entity_name": "IL6",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:00:37.118466+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11492",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il6 has been classified as Red List (Low Evidence).",
"entity_name": "IL6",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:00:27.006052+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11492",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IL6 were changed from to {Crohn disease-associated growth failure} 266600; {Intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to} 108010; {Rheumatoid arthritis, systemic juvenile} 604302; {Kaposi sarcoma, susceptibility to} 148000; {Type 1 diabetes mellitus} 222100; {Type 2 diabetes mellitus} 125853",
"entity_name": "IL6",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:00:04.607269+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11491",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IL6 as Red List (low evidence)",
"entity_name": "IL6",
"entity_type": "gene"
},
{
"created": "2022-03-17T17:00:04.548462+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11491",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il6 has been classified as Red List (Low Evidence).",
"entity_name": "IL6",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:59:45.278589+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: IL6: Changed rating: RED",
"entity_name": "IL6",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:59:35.996282+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IL6: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: {Crohn disease-associated growth failure} 266600, {Intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to} 108010, {Rheumatoid arthritis, systemic juvenile} 604302, {Kaposi sarcoma, susceptibility to} 148000, {Type 1 diabetes mellitus} 222100, {Type 2 diabetes mellitus} 125853; Mode of inheritance: None",
"entity_name": "IL6",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:55:07.069828+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL4 as ready",
"entity_name": "IL4",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:55:07.060038+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il4 has been classified as Red List (Low Evidence).",
"entity_name": "IL4",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:54:58.267148+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IL4 as Red List (low evidence)",
"entity_name": "IL4",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:54:58.255256+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il4 has been classified as Red List (Low Evidence).",
"entity_name": "IL4",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:54:39.371249+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IL4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "IL4",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:53:48.469102+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL36RN as ready",
"entity_name": "IL36RN",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:53:48.459340+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il36rn has been classified as Green List (High Evidence).",
"entity_name": "IL36RN",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:53:40.254087+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IL36RN were changed from to Psoriasis 14, pustular, MIM# 614204",
"entity_name": "IL36RN",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:53:14.670906+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11488",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IL36RN were set to ",
"entity_name": "IL36RN",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:52:51.624421+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11487",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL36RN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL36RN",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:52:29.999742+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IL36RN: Rating: GREEN; Mode of pathogenicity: None; Publications: 21848462, 21839423, 22903787, 23648549; Phenotypes: Psoriasis 14, pustular, MIM# 614204; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL36RN",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:48:51.986159+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL31RA as ready",
"entity_name": "IL31RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:48:51.975757+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il31ra has been classified as Red List (Low Evidence).",
"entity_name": "IL31RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:48:01.400913+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IL31RA were changed from to Amyloidosis, primary localized cutaneous, 2, MIM# 613955",
"entity_name": "IL31RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:47:36.265533+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL31RA was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "IL31RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:47:17.084741+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IL31RA as Red List (low evidence)",
"entity_name": "IL31RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:47:17.059611+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il31ra has been classified as Red List (Low Evidence).",
"entity_name": "IL31RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T16:46:52.572230+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IL31RA: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Amyloidosis, primary localized cutaneous, 2, MIM# 613955; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "IL31RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T11:31:16.540429+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.408",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2022-03-17T11:31:03.246778+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1487",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2022-03-17T11:30:54.843979+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.715",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2022-03-17T11:30:34.567153+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11483",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NDUFAF2: Rating: GREEN; Mode of pathogenicity: None; Publications: 33528536, 34364746, 16200211, 19384974, 20571988; Phenotypes: Mitochondrial complex I deficiency, nuclear type 10 - MIM#618233; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF2",
"entity_type": "gene"
},
{
"created": "2022-03-17T11:27:54.018447+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.408",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NDUFAF1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T11:27:19.577976+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.715",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NDUFAF1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T11:27:06.721120+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11483",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NDUFAF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17557076, 21931170, 16218961, 24963768, 34975718; Phenotypes: Mitochondrial complex I deficiency, nuclear type 11 - MIM#618234; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFAF1",
"entity_type": "gene"
},
{
"created": "2022-03-17T11:13:22.423036+11:00",
"panel_name": "Callosome",
"panel_id": 205,
"panel_version": "0.368",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NDUFA9: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T11:12:53.146322+11:00",
"panel_name": "Regression",
"panel_id": 206,
"panel_version": "0.408",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NDUFA9: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T11:11:45.386312+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11483",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NDUFA9: Rating: GREEN; Mode of pathogenicity: None; Publications: 26425749, 28671271, 22114105; Phenotypes: Mitochondrial complex I deficiency, nuclear type 26 - MIM#618247; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDUFA9",
"entity_type": "gene"
},
{
"created": "2022-03-17T10:50:54.396975+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11483",
"user_name": "Krithika Murali",
"item_type": "entity",
"text": "reviewed gene: NDUFA7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "NDUFA7",
"entity_type": "gene"
},
{
"created": "2022-03-17T10:26:04.053068+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11483",
"user_name": "Michelle Torres",
"item_type": "entity",
"text": "reviewed gene: TPTE2P5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "TPTE2P5",
"entity_type": "gene"
},
{
"created": "2022-03-17T08:46:33.377757+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL2RA as ready",
"entity_name": "IL2RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T08:46:33.363677+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il2ra has been classified as Green List (High Evidence).",
"entity_name": "IL2RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T08:46:23.970460+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IL2RA were changed from to Immunodeficiency 41 with lymphoproliferation and autoimmunity, MIM# 606367",
"entity_name": "IL2RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T08:46:01.078902+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11482",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IL2RA were set to ",
"entity_name": "IL2RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T08:45:38.096178+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11481",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IL2RA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL2RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T08:45:16.175997+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11480",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IL2RA: Rating: GREEN; Mode of pathogenicity: None; Publications: 9096364, 17196245, 23416241, 24116927; Phenotypes: Immunodeficiency 41 with lymphoproliferation and autoimmunity, MIM# 606367; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IL2RA",
"entity_type": "gene"
},
{
"created": "2022-03-17T08:27:53.035749+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL1RN as ready",
"entity_name": "IL1RN",
"entity_type": "gene"
},
{
"created": "2022-03-17T08:27:53.023518+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il1rn has been classified as Green List (High Evidence).",
"entity_name": "IL1RN",
"entity_type": "gene"
},
{
"created": "2022-03-17T08:27:50.575770+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.134",
"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": "2022-03-17T08:24:44.854565+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IL1RN were set to ",
"entity_name": "IL1RN",
"entity_type": "gene"
},
{
"created": "2022-03-17T08:24:14.165735+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.132",
"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": "2022-03-17T08:23:41.671483+11:00",
"panel_name": "Systemic Autoinflammatory Disease_Periodic Fever",
"panel_id": 238,
"panel_version": "0.131",
"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": "2022-03-17T08:22:54.232915+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11480",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL1RN as ready",
"entity_name": "IL1RN",
"entity_type": "gene"
},
{
"created": "2022-03-17T08:22:54.220867+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11480",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il1rn has been classified as Green List (High Evidence).",
"entity_name": "IL1RN",
"entity_type": "gene"
}
]
}