HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220759,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1590",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1588",
"results": [
{
"created": "2020-09-15T13:45:26.970375+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC37A4 were changed from to Glycogen storage disease Ib, MIM# 232220",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:44:59.279327+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC37A4 were set to ",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:44:35.214199+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC37A4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:44:11.319633+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC37A4: Rating: GREEN; Mode of pathogenicity: None; Publications: 31788408, 31536830; Phenotypes: Glycogen storage disease Ib, MIM# 232220; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC37A4",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:39:56.942120+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A38 as ready",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:39:56.930960+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a38 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:39:44.860008+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A38 were changed from to Anemia, sideroblastic, 2, pyridoxine-refractory, MIM# 205950",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:39:23.951305+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A38 were set to ",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:39:06.315827+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4435",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC25A38 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:38:50.329006+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC25A38: Rating: GREEN; Mode of pathogenicity: None; Publications: 19412178; Phenotypes: Anemia, sideroblastic, 2, pyridoxine-refractory, MIM# 205950; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:38:27.400860+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A38 as ready",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:38:27.389972+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a38 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:37:58.217124+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A38 were changed from to Anemia, sideroblastic, 2, pyridoxine-refractory, MIM# 205950",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:37:31.173357+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A38 were set to ",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:37:06.784777+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC25A38 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:36:35.896198+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC25A38: Rating: GREEN; Mode of pathogenicity: None; Publications: 19412178; Phenotypes: Anemia, sideroblastic, 2, pyridoxine-refractory, MIM# 205950; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:35:14.538421+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC19A2 as ready",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:35:14.527347+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc19a2 has been classified as Green List (High Evidence).",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:35:10.018544+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC19A2 as Green List (high evidence)",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:35:10.007897+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.389",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc19a2 has been classified as Green List (High Evidence).",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:34:45.503575+10:00",
"panel_name": "Deafness_IsolatedAndComplex",
"panel_id": 209,
"panel_version": "0.388",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC19A2 was added\ngene: SLC19A2 was added to Deafness_IsolatedAndComplex. Sources: Expert Review\nMode of inheritance for gene: SLC19A2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC19A2 were set to 10391221; 10978358\nPhenotypes for gene: SLC19A2 were set to Thiamine-responsive megaloblastic anemia syndrome, MIM# 249270\nReview for gene: SLC19A2 was set to GREEN\nAdded comment: Over 5 unrelated families reported, sensorineural deafness is part of the phenotype. \nSources: Expert Review",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:33:21.249484+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC19A2 as ready",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:33:21.236774+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc19a2 has been classified as Green List (High Evidence).",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:33:14.615661+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC19A2 were changed from to Thiamine-responsive megaloblastic anemia syndrome, MIM# 249270",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:32:58.874590+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC19A2 were set to ",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:32:42.515526+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4432",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC19A2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:32:24.104801+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4431",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC19A2: Rating: GREEN; Mode of pathogenicity: None; Publications: 10391221, 10978358; Phenotypes: Thiamine-responsive megaloblastic anemia syndrome, MIM# 249270; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:31:10.167568+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC19A2 as ready",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:31:10.158876+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc19a2 has been classified as Green List (High Evidence).",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:31:07.980969+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC19A2 were changed from to Thiamine-responsive megaloblastic anemia syndrome, MIM# 249270",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:30:40.812844+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC19A2 were set to ",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:30:17.692428+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC19A2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T13:29:52.468081+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC19A2: Rating: GREEN; Mode of pathogenicity: None; Publications: 10391221, 10978358; Phenotypes: Thiamine-responsive megaloblastic anemia syndrome, MIM# 249270; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC19A2",
"entity_type": "gene"
},
{
"created": "2020-09-15T11:04:33.926893+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATP7B as Amber List (moderate evidence)",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2020-09-15T11:04:33.918618+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp7b has been classified as Amber List (Moderate Evidence).",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2020-09-15T11:04:09.619816+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: In a recent cohort of 82 affected individuals, movement disorders were noted in 78/82 (95.1%) patients and included dystonia in 69 (84.1%), chorea in 31 (37.8%), tremor in 24 (29.3%), parkinsonism in 19 (23.2%), athetosis in 13 (15.9%), and myoclonus in 9 (11.0%) patients. Dystonia was more frequently observed in the patients with thalamic (76.8 vs 23.2%), globus pallidus (72.0 vs 28.0%), putamen (69.5 vs 30.5%), caudate (68.3 vs 31.7%) and brainstem (61.0 vs 39.0%) involvement, and tremor with cerebellar involvement (37.5 vs 5.2%).\r\n\r\nParoxysmal dyskinesia does not appear to be a common feature, and the gene is already included in the Dystonia_Complex panel.; to: In a recent cohort of 82 affected individuals, movement disorders were noted in 78/82 (95.1%) patients and included dystonia in 69 (84.1%), chorea in 31 (37.8%), tremor in 24 (29.3%), parkinsonism in 19 (23.2%), athetosis in 13 (15.9%), and myoclonus in 9 (11.0%) patients. Dystonia was more frequently observed in the patients with thalamic (76.8 vs 23.2%), globus pallidus (72.0 vs 28.0%), putamen (69.5 vs 30.5%), caudate (68.3 vs 31.7%) and brainstem (61.0 vs 39.0%) involvement, and tremor with cerebellar involvement (37.5 vs 5.2%).\r\n\r\nParoxysmal dyskinesia does not appear to be a common feature, and the gene is already included in the Dystonia_Complex panel. However, there are rare reports and this is a treatable disorder.",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2020-09-15T11:03:37.110979+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: ATP7B: Changed rating: AMBER",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2020-09-15T06:45:42.218394+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4431",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SEC23B as ready",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-15T06:45:42.206931+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4431",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sec23b has been classified as Green List (High Evidence).",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-15T06:45:33.563080+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4431",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SEC23B were changed from to Dyserythropoietic anemia, congenital, type II , MIM#224100",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:40:33.388626+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SEC23B were set to ",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:40:15.472638+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4429",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SEC23B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:39:54.025380+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "commented on gene: SEC23B: Over 20 families reported.",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:39:37.880668+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SEC23B: Rating: GREEN; Mode of pathogenicity: None; Publications: 19561605, 19621418; Phenotypes: Dyserythropoietic anemia, congenital, type II , MIM#224100; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:38:48.862171+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SEC23B as ready",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:38:48.853164+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sec23b has been classified as Green List (High Evidence).",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:38:43.115568+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SEC23B were changed from to Dyserythropoietic anemia, congenital, type II , MIM#224100",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:38:14.057970+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SEC23B were set to ",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:37:50.726210+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SEC23B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:37:22.323170+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SEC23B: Rating: GREEN; Mode of pathogenicity: None; Publications: 19561605, 19621418; Phenotypes: Dyserythropoietic anemia, congenital, type II , MIM#224100; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:35:17.024382+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RUNX1 as ready",
"entity_name": "RUNX1",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:35:17.013424+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: runx1 has been classified as Green List (High Evidence).",
"entity_name": "RUNX1",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:35:14.192471+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RUNX1 were changed from to Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399",
"entity_name": "RUNX1",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:34:55.375174+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RUNX1 were set to ",
"entity_name": "RUNX1",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:34:26.150006+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RUNX1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RUNX1",
"entity_type": "gene"
},
{
"created": "2020-09-14T21:34:00.485523+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RUNX1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10508512, 11830488; Phenotypes: Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RUNX1",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:28:47.713822+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS27 as ready",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:28:47.700234+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps27 has been classified as Red List (Low Evidence).",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:28:40.076932+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS27 were changed from to Diamond-Blackfan anemia 17, MIM# 617409",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:28:15.868836+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPS27 were set to ",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:27:57.635773+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS27 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:27:40.985323+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4425",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RPS27 as Red List (low evidence)",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:27:40.976813+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4425",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps27 has been classified as Red List (Low Evidence).",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:27:24.976029+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RPS27: Rating: RED; Mode of pathogenicity: None; Publications: 25424902; Phenotypes: Diamond-Blackfan anemia 17, MIM# 617409; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:26:43.731698+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS27 as ready",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:26:43.723931+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps27 has been classified as Red List (Low Evidence).",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:26:41.405088+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.28",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS27 were changed from to Diamond-Blackfan anemia 17, MIM# 617409",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:26:16.083114+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPS27 were set to ",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:25:59.172585+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS27 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:25:38.574878+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RPS27 as Red List (low evidence)",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:25:38.552318+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps27 has been classified as Red List (Low Evidence).",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:25:08.626314+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RPS27: Rating: RED; Mode of pathogenicity: None; Publications: 25424902; Phenotypes: Diamond-Blackfan anemia 17, MIM# 617409; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:24:24.665111+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS27 as ready",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:24:24.656345+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps27 has been classified as Red List (Low Evidence).",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:24:20.869987+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS27 were changed from to Diamond-Blackfan anemia 17, MIM# 617409",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:23:54.821369+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPS27 were set to ",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:23:33.660975+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS27 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:23:09.575221+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: RPS27 as Red List (low evidence)",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:23:09.566812+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps27 has been classified as Red List (Low Evidence).",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:22:47.025725+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RPS27: Rating: RED; Mode of pathogenicity: None; Publications: 25424902; Phenotypes: Diamond-Blackfan anemia 17, MIM# 617409; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS27",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:19:08.955910+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS17 as ready",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:19:08.945632+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps17 has been classified as Green List (High Evidence).",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:19:06.412538+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.73",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS17 were changed from to Diamond-Blackfan anemia 4, MIM# 612527",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:18:41.964389+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS17 as ready",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:18:41.955858+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps17 has been classified as Green List (High Evidence).",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:18:16.270000+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS17 were changed from to Diamond-Blackfan anemia 4, MIM# 612527",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:18:16.240937+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.72",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPS17 were set to ",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:17:55.669656+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.71",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS17 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:17:54.849871+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4423",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPS17 were set to ",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:17:34.951078+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4422",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS17 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:17:21.498727+10:00",
"panel_name": "Radial Ray Abnormalities",
"panel_id": 163,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RPS17: Rating: GREEN; Mode of pathogenicity: None; Publications: 17647292, 19061985, 23812780, 23718193; Phenotypes: Diamond-Blackfan anemia 4, MIM# 612527; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:17:17.369459+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4421",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RPS17: Rating: GREEN; Mode of pathogenicity: None; Publications: 17647292, 19061985, 23812780, 23718193; Phenotypes: Diamond-Blackfan anemia 4, MIM# 612527; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:16:08.795267+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS17 as ready",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:16:08.784594+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps17 has been classified as Green List (High Evidence).",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:16:02.426174+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RPS17 were changed from to Diamond-Blackfan anemia 4, MIM# 612527",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:15:42.501702+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RPS17 were set to ",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:15:18.766974+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: RPS17 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:14:51.015024+10:00",
"panel_name": "Diamond Blackfan anaemia",
"panel_id": 98,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: RPS17: Rating: GREEN; Mode of pathogenicity: None; Publications: 17647292, 19061985, 23812780, 23718193; Phenotypes: Diamond-Blackfan anemia 4, MIM# 612527; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:14:36.318986+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RPS17 as ready",
"entity_name": "RPS17",
"entity_type": "gene"
},
{
"created": "2020-09-14T20:14:36.306541+10:00",
"panel_name": "Bone Marrow Failure",
"panel_id": 56,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rps17 has been classified as Green List (High Evidence).",
"entity_name": "RPS17",
"entity_type": "gene"
}
]
}