HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220363,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2064",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2062",
"results": [
{
"created": "2019-12-06T21:06:55.976531+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: C19orf12 were changed from to Neurodegeneration with brain iron accumulation 4, MIM#614298",
"entity_name": "C19orf12",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:06:41.869058+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: C19orf12 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "C19orf12",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:06:33.958062+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: C19orf12 as Red List (low evidence)",
"entity_name": "C19orf12",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:06:33.950479+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: c19orf12 has been classified as Red List (Low Evidence).",
"entity_name": "C19orf12",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:05:47.741254+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BSND as ready",
"entity_name": "BSND",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:05:47.733874+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bsnd has been classified as Green List (High Evidence).",
"entity_name": "BSND",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:05:37.973998+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BSND were changed from to Bartter syndrome, type 4a, MIM#602522",
"entity_name": "BSND",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:05:17.377770+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BSND was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BSND",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:04:35.732820+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BRAT1 as ready",
"entity_name": "BRAT1",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:04:35.725391+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: brat1 has been classified as Green List (High Evidence).",
"entity_name": "BRAT1",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:04:28.643267+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BRAT1 were changed from to Neurodevelopmental disorder with cerebellar atrophy and with or without seizures, MIM#618056",
"entity_name": "BRAT1",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:04:16.354479+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BRAT1 were set to ",
"entity_name": "BRAT1",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:04:00.268229+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BRAT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BRAT1",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:03:31.679791+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BMPER as ready",
"entity_name": "BMPER",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:03:31.672807+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bmper has been classified as Green List (High Evidence).",
"entity_name": "BMPER",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:03:27.079431+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BMPER were changed from to Diaphanospondylodysostosis, MIM#608022",
"entity_name": "BMPER",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:03:15.273849+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.739",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BMPER was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BMPER",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:02:37.904584+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BICD2 as ready",
"entity_name": "BICD2",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:02:37.897267+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bicd2 has been classified as Red List (Low Evidence).",
"entity_name": "BICD2",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:02:28.387596+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BICD2 were changed from to Spinal muscular atrophy, lower extremity-predominant, 2A, autosomal dominant, MIM#615290",
"entity_name": "BICD2",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:02:16.330400+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.737",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BICD2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BICD2",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:01:57.728451+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BICD2 as Red List (low evidence)",
"entity_name": "BICD2",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:01:57.721520+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bicd2 has been classified as Red List (Low Evidence).",
"entity_name": "BICD2",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:01:01.483489+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BDNF as ready",
"entity_name": "BDNF",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:01:01.475885+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bdnf has been classified as Red List (Low Evidence).",
"entity_name": "BDNF",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:00:40.209331+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BDNF were changed from to Central hypoventilation syndrome, congenital, MIM#209880",
"entity_name": "BDNF",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:00:23.486923+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.734",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BDNF was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BDNF",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:00:13.941165+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BDNF as Red List (low evidence)",
"entity_name": "BDNF",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:00:13.932004+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bdnf has been classified as Red List (Low Evidence).",
"entity_name": "BDNF",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:59:41.986053+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.732",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBIP1 as ready",
"entity_name": "BBIP1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:59:41.979053+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.732",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbip1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "BBIP1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:59:33.923597+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.732",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBIP1 were changed from to Bardet-Biedl syndrome 18, MIM#615995",
"entity_name": "BBIP1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:59:20.089620+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.731",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBIP1 were set to ",
"entity_name": "BBIP1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:59:10.462396+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.730",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBIP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBIP1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:58:54.362102+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.729",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BBIP1 as Amber List (moderate evidence)",
"entity_name": "BBIP1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:58:54.354717+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.729",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbip1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "BBIP1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:58:19.146323+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.728",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: B9D2 as ready",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:58:19.139097+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.728",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b9d2 has been classified as Green List (High Evidence).",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:58:01.529213+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.728",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: B9D2 were changed from to Joubert syndrome 34, MIM#614175; Meckel syndrome 10, MIM#614175",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:57:47.300804+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.727",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: B9D2 were set to ",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:57:34.640629+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.726",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: B9D2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "B9D2",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:56:59.031685+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.725",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: B9D1 as ready",
"entity_name": "B9D1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:56:59.024503+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.725",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b9d1 has been classified as Green List (High Evidence).",
"entity_name": "B9D1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:56:43.825668+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.725",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: B9D1 were changed from to Joubert syndrome 27, MIM#617120; Meckel syndrome 9, MIM#614209",
"entity_name": "B9D1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:56:29.313261+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.724",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: B9D1 were set to ",
"entity_name": "B9D1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:56:14.413006+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.723",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: B9D1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "B9D1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:16:24.616548+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.722",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: B4GALT1 as ready",
"entity_name": "B4GALT1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:16:24.609517+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.722",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b4galt1 has been classified as Green List (High Evidence).",
"entity_name": "B4GALT1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:16:18.685816+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.722",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: B4GALT1 were changed from to Congenital disorder of glycosylation, type Iid, MIM#607091",
"entity_name": "B4GALT1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:16:05.088633+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.721",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: B4GALT1 were set to ",
"entity_name": "B4GALT1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:15:52.882289+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.720",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: B4GALT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "B4GALT1",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:15:14.958582+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.719",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: B3GAT3 as ready",
"entity_name": "B3GAT3",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:15:14.950723+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.719",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b3gat3 has been classified as Red List (Low Evidence).",
"entity_name": "B3GAT3",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:15:10.356556+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.719",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: B3GAT3 were changed from to Multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects, MIM#245600",
"entity_name": "B3GAT3",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:14:55.565525+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.718",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: B3GAT3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "B3GAT3",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:14:48.098100+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.717",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: B3GAT3 as Red List (low evidence)",
"entity_name": "B3GAT3",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:14:48.089964+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.717",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b3gat3 has been classified as Red List (Low Evidence).",
"entity_name": "B3GAT3",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:13:57.284355+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.716",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: B3GALT6 as ready",
"entity_name": "B3GALT6",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:13:57.276673+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.716",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b3galt6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "B3GALT6",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:08:04.093704+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.716",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: B3GALT6 were changed from to Ehlers-Danlos syndrome, spondylodysplastic type, 2, MIM#615349; Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures, MIM#271640",
"entity_name": "B3GALT6",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:07:52.413554+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.715",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: B3GALT6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "B3GALT6",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:07:30.645587+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.714",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: B3GALT6 as Amber List (moderate evidence)",
"entity_name": "B3GALT6",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:07:30.637894+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.714",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b3galt6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "B3GALT6",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:06:28.792414+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.713",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AHCY as ready",
"entity_name": "AHCY",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:06:28.785223+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.713",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ahcy has been classified as Green List (High Evidence).",
"entity_name": "AHCY",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:06:24.582894+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.713",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AHCY were changed from to Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase, MIM#613752",
"entity_name": "AHCY",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:06:11.649149+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.712",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AHCY was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AHCY",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:00:56.258255+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ASNS as ready",
"entity_name": "ASNS",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:00:56.251220+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: asns has been classified as Green List (High Evidence).",
"entity_name": "ASNS",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:00:46.570257+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ASNS were changed from to Asparagine synthetase deficiency, MIM#615574",
"entity_name": "ASNS",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:00:09.822329+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.710",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ASL as ready",
"entity_name": "ASL",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:00:09.813755+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.710",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: asl has been classified as Green List (High Evidence).",
"entity_name": "ASL",
"entity_type": "gene"
},
{
"created": "2019-12-06T20:00:04.973780+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.710",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ASL were changed from to Argininosuccinic aciduria, MIM#207900",
"entity_name": "ASL",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:59:52.332297+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.709",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ASL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ASL",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:58:52.525920+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALX3 as ready",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:58:52.518528+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alx3 has been classified as Green List (High Evidence).",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:58:48.378610+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ALX3 were changed from to Frontonasal dysplasia 1, MIM#136760",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:58:35.365407+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.707",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ALX3 were set to ",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:58:23.193269+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.706",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ALX3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALX3",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:57:52.090231+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALX1 as ready",
"entity_name": "ALX1",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:57:52.083045+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alx1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ALX1",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:57:45.234868+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.705",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ALX1 were changed from to Frontonasal dysplasia 3, MIM#613456",
"entity_name": "ALX1",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:57:31.470551+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.704",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ALX1 were set to ",
"entity_name": "ALX1",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:57:18.837105+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.703",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ALX1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALX1",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:57:03.580665+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.702",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ALX1 as Amber List (moderate evidence)",
"entity_name": "ALX1",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:57:03.573447+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.702",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alx1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ALX1",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:56:32.061130+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.701",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALG14 as ready",
"entity_name": "ALG14",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:56:32.054150+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.701",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alg14 has been classified as Green List (High Evidence).",
"entity_name": "ALG14",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:56:26.974710+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.701",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ALG14 were changed from to Myasthenic syndrome, congenital, 15, without tubular aggregates, MIM#616227; Intellectual disability",
"entity_name": "ALG14",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:56:14.342048+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.700",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ALG14 were set to ",
"entity_name": "ALG14",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:56:00.000356+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.699",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ALG14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALG14",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:55:15.184906+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.698",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALDOB as ready",
"entity_name": "ALDOB",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:55:15.177759+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.698",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aldob has been classified as Green List (High Evidence).",
"entity_name": "ALDOB",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:55:04.495445+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.698",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ALDOB were changed from to Fructose intolerance, hereditary, MIM#229600",
"entity_name": "ALDOB",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:54:52.460710+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.697",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ALDOB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ALDOB",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:53:29.709872+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.696",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AGA as ready",
"entity_name": "AGA",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:53:29.702842+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.696",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aga has been classified as Green List (High Evidence).",
"entity_name": "AGA",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:53:25.328517+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.696",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AGA were changed from to Aspartylglucosaminuria, MIM#208400",
"entity_name": "AGA",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:53:11.584984+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.695",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AGA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "AGA",
"entity_type": "gene"
},
{
"created": "2019-12-06T19:52:33.934718+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.694",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADD3 as ready",
"entity_name": "ADD3",
"entity_type": "gene"
}
]
}