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{
"count": 221415,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=547",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=545",
"results": [
{
"created": "2023-09-18T18:09:05.093029+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ABAT as Amber List (moderate evidence)",
"entity_name": "ABAT",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:09:05.079667+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: abat has been classified as Amber List (Moderate Evidence).",
"entity_name": "ABAT",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:08:21.597367+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE2A were set to 32467598; 32196122; 29392776",
"entity_name": "PDE2A",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:07:28.784601+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: XPR1 as ready",
"entity_name": "XPR1",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:07:28.768277+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpr1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "XPR1",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:07:26.042903+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: XPR1 were changed from brain calcification; basal ganglia calcification; paroxysmal dyskinesia; epilepsy; DEE to Basal ganglia calcification, idiopathic, 6, MIM# 616413; brain calcification; basal ganglia calcification; paroxysmal dyskinesia; epilepsy; DEE",
"entity_name": "XPR1",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:06:53.120427+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: XPR1 as Amber List (moderate evidence)",
"entity_name": "XPR1",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:06:53.109565+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xpr1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "XPR1",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:06:03.873197+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLDN5 as ready",
"entity_name": "CLDN5",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:06:03.857931+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cldn5 has been classified as Green List (High Evidence).",
"entity_name": "CLDN5",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:06:00.334083+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CLDN5 as Green List (high evidence)",
"entity_name": "CLDN5",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:06:00.323289+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cldn5 has been classified as Green List (High Evidence).",
"entity_name": "CLDN5",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:05:32.423647+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLDN5 were changed from familial migraine; alternating hemiplegia; hemiplegic migraine; brain calcification; acquired microcephaly; epilepsy to Syndromic disorder, MONDO:0002254, CLDN5-related; familial migraine; alternating hemiplegia; hemiplegic migraine; brain calcification; acquired microcephaly; epilepsy",
"entity_name": "CLDN5",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:05:08.406219+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CLDN5 as Green List (high evidence)",
"entity_name": "CLDN5",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:05:08.393112+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cldn5 has been classified as Green List (High Evidence).",
"entity_name": "CLDN5",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:04:08.445132+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIAA1161 as ready",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:04:08.434391+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kiaa1161 has been classified as Green List (High Evidence).",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:04:05.447185+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KIAA1161 were changed from paroxysmal dyskinesia; brain calcification; episodic hemiparesis to Basal ganglia calcification, idiopathic, 7, autosomal recessive, OMIM #618317; paroxysmal dyskinesia; brain calcification; episodic hemiparesis",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:03:21.800430+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KIAA1161 as Green List (high evidence)",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:03:21.792123+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kiaa1161 has been classified as Green List (High Evidence).",
"entity_name": "KIAA1161",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:02:29.415296+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKN as ready",
"entity_name": "PRKN",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:02:29.406172+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkn has been classified as Amber List (Moderate Evidence).",
"entity_name": "PRKN",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:02:26.859109+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PRKN were changed from paroxysmal exercise induced dyskinesia; fasting induced dyskinesia; early onset parkinsonism to Parkinson disease, juvenile, type 2 MIM#600116; paroxysmal exercise induced dyskinesia; fasting induced dyskinesia; early onset parkinsonism",
"entity_name": "PRKN",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:01:47.139346+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PRKN as Amber List (moderate evidence)",
"entity_name": "PRKN",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:01:47.124070+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkn has been classified as Amber List (Moderate Evidence).",
"entity_name": "PRKN",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:00:52.854028+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NBEA as ready",
"entity_name": "NBEA",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:00:52.842721+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nbea has been classified as Amber List (Moderate Evidence).",
"entity_name": "NBEA",
"entity_type": "gene"
},
{
"created": "2023-09-18T18:00:37.867745+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NBEA were changed from Paroxysmal Kinesigenic Dyskinesia; DEE; autism; intellectual disability to Neurodevelopmental disorder with or without early-onset generalized epilepsy, MIM# 619157; Paroxysmal Kinesigenic Dyskinesia; DEE; autism; intellectual disability",
"entity_name": "NBEA",
"entity_type": "gene"
},
{
"created": "2023-09-18T17:59:48.629762+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NBEA as Amber List (moderate evidence)",
"entity_name": "NBEA",
"entity_type": "gene"
},
{
"created": "2023-09-18T17:59:48.621835+10:00",
"panel_name": "Paroxysmal Dyskinesia",
"panel_id": 259,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nbea has been classified as Amber List (Moderate Evidence).",
"entity_name": "NBEA",
"entity_type": "gene"
},
{
"created": "2023-09-18T17:58:51.592696+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5472",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBB3 as ready",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2023-09-18T17:58:51.578693+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5472",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubb3 has been classified as Green List (High Evidence).",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2023-09-18T17:57:55.508748+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5472",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBB3 were changed from to complex cortical dysplasia with other brain malformations 1 MONDO:0013541",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2023-09-18T17:57:11.749323+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBB3 were set to ",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2023-09-18T17:53:42.387442+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5470",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TUBB3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2023-09-18T17:48:10.272362+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBB4A as ready",
"entity_name": "TUBB4A",
"entity_type": "gene"
},
{
"created": "2023-09-18T17:48:10.260591+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubb4a has been classified as Green List (High Evidence).",
"entity_name": "TUBB4A",
"entity_type": "gene"
},
{
"created": "2023-09-18T17:47:11.372913+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBB4A were changed from to hypomyelinating leukodystrophy 6 MONDO:0012905",
"entity_name": "TUBB4A",
"entity_type": "gene"
},
{
"created": "2023-09-18T17:46:25.174142+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5468",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBB4A were set to ",
"entity_name": "TUBB4A",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:36:30.795609+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5467",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TUBB4A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TUBB4A",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:30:21.620656+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5466",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TH as ready",
"entity_name": "TH",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:30:21.610337+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5466",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: th has been classified as Green List (High Evidence).",
"entity_name": "TH",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:30:16.133811+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5466",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TH were changed from to Segawa syndrome, recessive MIM#605407",
"entity_name": "TH",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:29:42.009204+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5465",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TH were set to ",
"entity_name": "TH",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:28:39.911482+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5464",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TH",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:28:05.589557+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5463",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag treatable tag was added to gene: TH.",
"entity_name": "TH",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:27:34.854646+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5463",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTEN as ready",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:27:34.840411+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5463",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pten has been classified as Green List (High Evidence).",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:26:59.403617+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5463",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PTEN were changed from to Cowden syndrome 1 MIM#158350; Macrocephaly/autism syndrome MIM#605309",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:24:50.671325+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5462",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PTEN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:23:58.798364+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5461",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBG1 as ready",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:23:58.788936+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5461",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubg1 has been classified as Green List (High Evidence).",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:23:54.241193+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5461",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBG1 were changed from to complex cortical dysplasia with other brain malformations 4 MONDO:0014171",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:23:15.954523+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5460",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBG1 were set to ",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:22:41.566562+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5459",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TUBG1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:21:56.244992+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5458",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TWIST1 as ready",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:21:56.225515+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5458",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: twist1 has been classified as Green List (High Evidence).",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:21:50.911265+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5458",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TWIST1 were changed from to Saethre-Chotzen syndrome MONDO:0007042",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:21:16.759649+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5457",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TWIST1 were set to ",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:20:39.028471+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5456",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TWIST1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TWIST1",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:19:53.438988+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5455",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBA5 as ready",
"entity_name": "UBA5",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:19:53.427516+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5455",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: uba5 has been classified as Green List (High Evidence).",
"entity_name": "UBA5",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:19:49.110400+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5455",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBA5 were changed from to Epileptic encephalopathy, early infantile, 44 (MIM#617132)",
"entity_name": "UBA5",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:19:21.292681+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5454",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBA5 were set to 33811063",
"entity_name": "UBA5",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:18:48.313027+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBA5 were set to ",
"entity_name": "UBA5",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:18:15.356000+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5452",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UBA5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "UBA5",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:17:31.982718+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5451",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBE3A as ready",
"entity_name": "UBE3A",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:17:31.971451+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5451",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ube3a has been classified as Green List (High Evidence).",
"entity_name": "UBE3A",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:17:28.022375+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5451",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: UBE3A were changed from to Angelman syndrome MONDO:0007113",
"entity_name": "UBE3A",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:16:55.235529+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5450",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: UBE3A were set to ",
"entity_name": "UBE3A",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:16:22.332807+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5449",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: UBE3A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)",
"entity_name": "UBE3A",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:15:31.068544+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5448",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHA as ready",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2023-09-18T16:15:31.056256+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5448",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdha has been classified as Green List (High Evidence).",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:57:08.763403+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5448",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SDHA were changed from to Mitochondrial complex II deficiency, nuclear type 1 MIM#252011",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:56:29.450361+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5447",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SDHA were set to ",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:55:49.270433+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5446",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SDHA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SDHA",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:54:58.850934+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VLDLR as ready",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:54:58.840489+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vldlr has been classified as Green List (High Evidence).",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:54:46.786705+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VLDLR were changed from to cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1 MONDO:0024542",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:52:01.209565+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: VLDLR were set to ",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:51:28.075105+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5443",
"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": "2023-09-18T15:50:39.588693+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VPS13B as ready",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:50:39.577860+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vps13b has been classified as Green List (High Evidence).",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:50:31.656489+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VPS13B were changed from to Cohen syndrome MONDO:0008999",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:49:58.298352+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: VPS13B were set to ",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2023-09-18T15:49:25.698855+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5440",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: VPS13B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "VPS13B",
"entity_type": "gene"
},
{
"created": "2023-09-18T14:52:45.529575+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1173",
"user_name": "Lucy Spencer",
"item_type": "entity",
"text": "reviewed gene: SEMA3E: Rating: AMBER; Mode of pathogenicity: None; Publications: 15235037, 31691538, 31464029, 35628442, 32441320; Phenotypes: CHARGE syndrome MONDO:0008965, SEMA3E-related; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SEMA3E",
"entity_type": "gene"
},
{
"created": "2023-09-17T15:55:59.502447+10:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SCAF4 were changed from Neurodevelopmental disorder MONDO#0700092, SCAF4-related to Fliedner-Zweier syndrome, MIM#620511",
"entity_name": "SCAF4",
"entity_type": "gene"
},
{
"created": "2023-09-17T15:55:44.874444+10:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SCAF4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fliedner-Zweier syndrome, MIM#620511; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SCAF4",
"entity_type": "gene"
},
{
"created": "2023-09-17T15:55:25.898658+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5439",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SCAF4 were changed from Mild intellectual disability; seizures; behavioral abnormalities to Fliedner-Zweier syndrome, MIM#620511",
"entity_name": "SCAF4",
"entity_type": "gene"
},
{
"created": "2023-09-17T15:54:51.863088+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SCAF4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fliedner-Zweier syndrome, MIM#620511; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SCAF4",
"entity_type": "gene"
},
{
"created": "2023-09-17T15:54:32.995828+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1917",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SCAF4 were changed from Mild intellectual disability; seizures; behavioral abnormalities to Fliedner-Zweier syndrome, MIM#620511",
"entity_name": "SCAF4",
"entity_type": "gene"
},
{
"created": "2023-09-17T15:53:54.150304+10:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1916",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SCAF4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fliedner-Zweier syndrome, MIM#620511; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SCAF4",
"entity_type": "gene"
},
{
"created": "2023-09-17T15:53:32.038752+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1173",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SCAF4 were changed from Mild intellectual disability; seizures; behavioral abnormalities to Fliedner-Zweier syndrome, MIM#620511",
"entity_name": "SCAF4",
"entity_type": "gene"
},
{
"created": "2023-09-17T15:53:06.569471+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.1172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SCAF4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Fliedner-Zweier syndrome, MIM#620511; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SCAF4",
"entity_type": "gene"
},
{
"created": "2023-09-16T16:47:31.047674+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: VRK1 as ready",
"entity_name": "VRK1",
"entity_type": "gene"
},
{
"created": "2023-09-16T16:47:31.034798+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: vrk1 has been classified as Green List (High Evidence).",
"entity_name": "VRK1",
"entity_type": "gene"
},
{
"created": "2023-09-16T16:44:02.553914+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: VRK1 were changed from to pontocerebellar hypoplasia type 1A MONDO:0011866",
"entity_name": "VRK1",
"entity_type": "gene"
},
{
"created": "2023-09-16T16:43:20.850117+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: VRK1 were set to ",
"entity_name": "VRK1",
"entity_type": "gene"
},
{
"created": "2023-09-16T16:42:53.568824+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.5436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: VRK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "VRK1",
"entity_type": "gene"
}
]
}