HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220842,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1961",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1959",
"results": [
{
"created": "2020-01-26T17:45:56.352603+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1686",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WARS2 was added\ngene: WARS2 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list\nMode of inheritance for gene: WARS2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: WARS2 were set to 29783990; 28236339; 29120065; 28650581; 28905505\nPhenotypes for gene: WARS2 were set to Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures, MIM#617710\nReview for gene: WARS2 was set to GREEN\ngene: WARS2 was marked as current diagnostic\nAdded comment: 7 unrelated families reported. \nSources: Expert list",
"entity_name": "WARS2",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:45:13.056077+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WARS2 as ready",
"entity_name": "WARS2",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:45:13.048188+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wars2 has been classified as Green List (High Evidence).",
"entity_name": "WARS2",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:44:38.088162+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: WARS2 as Green List (high evidence)",
"entity_name": "WARS2",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:44:38.081291+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wars2 has been classified as Green List (High Evidence).",
"entity_name": "WARS2",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:43:33.957074+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WARS2 was added\ngene: WARS2 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: WARS2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: WARS2 were set to 29783990; 28236339; 29120065; 28650581; 28905505\nPhenotypes for gene: WARS2 were set to Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures, MIM#617710\nReview for gene: WARS2 was set to GREEN\ngene: WARS2 was marked as current diagnostic\nAdded comment: 7 unrelated families reported, most affected individuals had seizures as part of this mitochondrial disorder. \nSources: Expert list",
"entity_name": "WARS2",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:39:48.559538+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1685",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VPS11 as ready",
"entity_name": "VPS11",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:39:48.552869+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1685",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vps11 has been classified as Green List (High Evidence).",
"entity_name": "VPS11",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:39:36.086028+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1685",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: VPS11 as Green List (high evidence)",
"entity_name": "VPS11",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:39:36.078522+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1685",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vps11 has been classified as Green List (High Evidence).",
"entity_name": "VPS11",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:38:39.966758+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VPS11 was added\ngene: VPS11 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list\nMode of inheritance for gene: VPS11 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: VPS11 were set to 27120463; 26307567; 27473128\nPhenotypes for gene: VPS11 were set to Leukodystrophy, hypomyelinating, 12, MIM#616683\nReview for gene: VPS11 was set to GREEN\nAdded comment: ID, (variable) acquired microcephaly with hypomyelination; seizures in several reported individuals. 13 individuals from 7 Ashkenazi Jewish families, homozygous for a founder mutation (NM_021729.5:c.2536T>G or p.Cys846Gly); a different variant (p.Leu387_Gly395del) reported in a consanguineous family. \nSources: Expert list",
"entity_name": "VPS11",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:37:57.613516+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VPS11 as ready",
"entity_name": "VPS11",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:37:57.605751+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vps11 has been classified as Green List (High Evidence).",
"entity_name": "VPS11",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:37:10.046606+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: VPS11 as Green List (high evidence)",
"entity_name": "VPS11",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:37:10.034020+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vps11 has been classified as Green List (High Evidence).",
"entity_name": "VPS11",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:35:55.992822+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.524",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VPS11 was added\ngene: VPS11 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: VPS11 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: VPS11 were set to 27120463; 26307567; 27473128\nPhenotypes for gene: VPS11 were set to Leukodystrophy, hypomyelinating, 12, MIM#616683\nReview for gene: VPS11 was set to GREEN\ngene: VPS11 was marked as current diagnostic\nAdded comment: ID, (variable) acquired microcephaly with hypomyelination; seizures in several reported individuals.\r\n\r\n13 individuals from 7 Ashkenazi Jewish families, homozygous for a founder mutation (NM_021729.5:c.2536T>G or p.Cys846Gly); a different variant (p.Leu387_Gly395del) reported in a consanguineous family. \nSources: Expert list",
"entity_name": "VPS11",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:35:31.679060+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VLDLR as ready",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:35:30.879050+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vldlr has been classified as Amber List (Moderate Evidence).",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:31:51.106092+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: VLDLR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:30:26.840018+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VLDLR were changed from to Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1, MIM#224050",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:29:56.243612+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: VLDLR were set to ",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:28:43.180268+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.521",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: VLDLR as Amber List (moderate evidence)",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:28:43.172048+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.521",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vldlr has been classified as Amber List (Moderate Evidence).",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:28:01.896600+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.520",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: VLDLR: Rating: AMBER; Mode of pathogenicity: None; Publications: 16174313, 18326629; Phenotypes: Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1, MIM#224050; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:25:37.469221+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.520",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VAMP2 as ready",
"entity_name": "VAMP2",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:25:37.461908+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.520",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vamp2 has been classified as Green List (High Evidence).",
"entity_name": "VAMP2",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:24:43.136446+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.520",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: VAMP2 as Green List (high evidence)",
"entity_name": "VAMP2",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:24:43.128423+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.520",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vamp2 has been classified as Green List (High Evidence).",
"entity_name": "VAMP2",
"entity_type": "gene"
},
{
"created": "2020-01-26T17:23:47.212196+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.519",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VAMP2 was added\ngene: VAMP2 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: VAMP2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: VAMP2 were set to 30929742\nPhenotypes for gene: VAMP2 were set to Cortical visual impairment; Seizures; Stereotypic behaviour; Generalized hypotonia; Intellectual disability\nReview for gene: VAMP2 was set to GREEN\ngene: VAMP2 was marked as current diagnostic\nAdded comment: Five unrelated individuals reported, three had seizures as part of the phenotype of this neurodevelopmental condition. \nSources: Expert list",
"entity_name": "VAMP2",
"entity_type": "gene"
},
{
"created": "2020-01-26T16:22:10.442246+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBB2A as ready",
"entity_name": "TUBB2A",
"entity_type": "gene"
},
{
"created": "2020-01-26T16:22:10.434911+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubb2a has been classified as Green List (High Evidence).",
"entity_name": "TUBB2A",
"entity_type": "gene"
},
{
"created": "2020-01-26T16:22:00.595535+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TUBB2A as Green List (high evidence)",
"entity_name": "TUBB2A",
"entity_type": "gene"
},
{
"created": "2020-01-26T16:22:00.588365+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubb2a has been classified as Green List (High Evidence).",
"entity_name": "TUBB2A",
"entity_type": "gene"
},
{
"created": "2020-01-26T16:21:01.532310+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.517",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBB2A was added\ngene: TUBB2A was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: TUBB2A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: TUBB2A were set to 24702957; 25326637\nPhenotypes for gene: TUBB2A were set to Cortical dysplasia, complex, with other brain malformations 5, MIM#615763\nReview for gene: TUBB2A was set to GREEN\ngene: TUBB2A was marked as current diagnostic\nAdded comment: Seizures are part of the phenotype of the tubulinopathies. \nSources: Expert list",
"entity_name": "TUBB2A",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:19:08.062868+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBA8 as ready",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:19:08.053985+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tuba8 has been classified as Green List (High Evidence).",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:19:00.124718+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBA8 were changed from Cortical dysplasia, complex, with other brain malformations 8, MIM#613180 to Cortical dysplasia, complex, with other brain malformations 8, MIM#613180",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:18:25.210625+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.515",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBA8 were changed from to Cortical dysplasia, complex, with other brain malformations 8, MIM#613180",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:17:51.796241+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBA8 were set to ",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:17:11.909635+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.513",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TUBA8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:16:30.950763+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TUBA8: Rating: GREEN; Mode of pathogenicity: None; Publications: 31481326, 19896110; Phenotypes: Cortical dysplasia, complex, with other brain malformations 8, MIM#613180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:14:22.358853+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSFM as ready",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:14:22.351514+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsfm has been classified as Green List (High Evidence).",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:14:12.961096+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSFM were changed from to Combined oxidative phosphorylation deficiency 3, MIM#610505",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:13:38.112593+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.511",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TSFM was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:12:54.672681+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.510",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TSFM: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Combined oxidative phosphorylation deficiency 3, MIM#610505; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:08:04.133880+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.510",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSEN2 as ready",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:08:04.123999+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.510",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsen2 has been classified as Green List (High Evidence).",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:07:52.598143+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.510",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSEN2 were changed from to Pontocerebellar hypoplasia, type 2F, MIM#617026",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:07:18.772224+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.509",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TSEN2 were set to ",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:06:41.017068+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TSEN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:05:58.815689+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.507",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TSEN2: Rating: GREEN; Mode of pathogenicity: None; Publications: 23562994, 18711368, 20952379; Phenotypes: Pontocerebellar hypoplasia, type 2F, MIM#617026; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TSEN2",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:02:23.482408+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.507",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRRAP as ready",
"entity_name": "TRRAP",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:02:23.475809+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.507",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trrap has been classified as Green List (High Evidence).",
"entity_name": "TRRAP",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:02:10.806137+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.507",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRRAP were changed from to Developmental delay with or without dysmorphic facies and autism, MIM#618454",
"entity_name": "TRRAP",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:01:35.000759+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.506",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRRAP were set to ",
"entity_name": "TRRAP",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:00:58.888125+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.505",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRRAP was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRRAP",
"entity_type": "gene"
},
{
"created": "2020-01-26T15:00:17.164304+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRRAP: Rating: GREEN; Mode of pathogenicity: None; Publications: 30827496, 28628100; Phenotypes: Developmental delay with or without dysmorphic facies and autism, MIM#618454; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRRAP",
"entity_type": "gene"
},
{
"created": "2020-01-26T14:47:05.932219+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRPM6 as ready",
"entity_name": "TRPM6",
"entity_type": "gene"
},
{
"created": "2020-01-26T14:47:05.925224+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trpm6 has been classified as Green List (High Evidence).",
"entity_name": "TRPM6",
"entity_type": "gene"
},
{
"created": "2020-01-26T14:46:57.235361+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRPM6 as Green List (high evidence)",
"entity_name": "TRPM6",
"entity_type": "gene"
},
{
"created": "2020-01-26T14:46:57.228355+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trpm6 has been classified as Green List (High Evidence).",
"entity_name": "TRPM6",
"entity_type": "gene"
},
{
"created": "2020-01-26T14:45:58.941458+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.503",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TRPM6 was added\ngene: TRPM6 was added to Genetic Epilepsy. Sources: Expert list\nMode of inheritance for gene: TRPM6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TRPM6 were set to Hypomagnesemia 1, intestinal, MIM#602014\nReview for gene: TRPM6 was set to GREEN\ngene: TRPM6 was marked as current diagnostic\nAdded comment: Can present with seizures. \nSources: Expert list",
"entity_name": "TRPM6",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:41:13.000482+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRAPPC12 as ready",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:41:12.993298+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc12 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:40:25.064210+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1683",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRAPPC12 as Green List (high evidence)",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:40:25.056381+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1683",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc12 has been classified as Green List (High Evidence).",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:39:54.234579+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on publications: Additional unpublished case reported by GEL.",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:39:54.204635+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRAPPC12 were set to 28777934",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:39:32.300840+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRAPPC12 as ready",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:39:31.935499+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Additional unpublished case reported by GEL PanelApp.",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:39:30.629237+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc12 has been classified as Green List (High Evidence).",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:39:23.391684+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRAPPC12 as Green List (high evidence)",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:39:23.360542+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc12 has been classified as Green List (High Evidence).",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:38:52.678529+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on publications: Additional unpublished case reported by GEL.",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:38:52.663510+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRAPPC12 were set to 28777934",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:38:21.115646+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRAPPC12 as Green List (high evidence)",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:38:21.083649+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc12 has been classified as Green List (High Evidence).",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:37:47.582495+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRAPPC12 were changed from Encephalopathy, progressive, early-onset, with brain atrophy and spasticity, MIM#617669 to Encephalopathy, progressive, early-onset, with brain atrophy and spasticity, MIM#617669",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:37:47.378228+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1681",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRAPPC12 were changed from to Encephalopathy, progressive, early-onset, with brain atrophy and spasticity, MIM#617669",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:36:58.402512+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRAPPC12 were changed from Encephalopathy, progressive, early-onset, with brain atrophy and spasticity, MIM#617669 to Encephalopathy, progressive, early-onset, with brain atrophy and spasticity, MIM#617669",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:36:53.325676+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1681",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRAPPC12 were set to ",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:35:57.791508+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.501",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRAPPC12 were changed from to Encephalopathy, progressive, early-onset, with brain atrophy and spasticity, MIM#617669",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:35:57.580619+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1681",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRAPPC12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:34:34.829416+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.501",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRAPPC12 were set to ",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:34:12.680059+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRAPPC12 as Amber List (moderate evidence)",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:34:12.671471+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc12 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:33:45.988190+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.500",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRAPPC12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:33:23.205056+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1679",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRAPPC12: Rating: AMBER; Mode of pathogenicity: None; Publications: 28777934; Phenotypes: Encephalopathy, progressive, early-onset, with brain atrophy and spasticity, MIM#617669; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:32:39.847385+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.499",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRAPPC12 as Amber List (moderate evidence)",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:32:39.840402+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.499",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trappc12 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:31:57.284283+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRAPPC12: Rating: AMBER; Mode of pathogenicity: None; Publications: 28777934; Phenotypes: Encephalopathy, progressive, early-onset, with brain atrophy and spasticity, MIM#617669; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TRAPPC12",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:29:57.063865+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRAF7 as ready",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:29:57.051608+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: traf7 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:29:48.389222+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRAF7 were changed from Cardiac, facial, and digital anomalies with developmental delay, MIM#618164 to Cardiac, facial, and digital anomalies with developmental delay, MIM#618164",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:29:14.554169+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.497",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRAF7 were changed from to Cardiac, facial, and digital anomalies with developmental delay, MIM#618164",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:28:41.238419+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRAF7 were set to ",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:28:08.483609+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.495",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TRAF7 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:27:20.931923+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRAF7 as Amber List (moderate evidence)",
"entity_name": "TRAF7",
"entity_type": "gene"
},
{
"created": "2020-01-25T20:27:20.924614+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: traf7 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TRAF7",
"entity_type": "gene"
}
]
}