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{
"count": 220489,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1536",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1534",
"results": [
{
"created": "2020-10-17T10:39:01.860016+11:00",
"panel_name": "Heterotaxy",
"panel_id": 108,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: CCDC103.",
"entity_name": "CCDC103",
"entity_type": "gene"
},
{
"created": "2020-10-17T10:38:52.197951+11:00",
"panel_name": "Heterotaxy",
"panel_id": 108,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CCDC103: Rating: GREEN; Mode of pathogenicity: None; Publications: 22581229, 32447765, 31858719, 28790179; Phenotypes: Ciliary dyskinesia, primary, 17, MIM# 614679; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CCDC103",
"entity_type": "gene"
},
{
"created": "2020-10-17T10:38:13.969914+11:00",
"panel_name": "Ciliary Dyskinesia",
"panel_id": 82,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: CCDC103.",
"entity_name": "CCDC103",
"entity_type": "gene"
},
{
"created": "2020-10-17T10:36:42.967512+11:00",
"panel_name": "Ciliary Dyskinesia",
"panel_id": 82,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CCDC103 as ready",
"entity_name": "CCDC103",
"entity_type": "gene"
},
{
"created": "2020-10-17T10:36:42.953624+11:00",
"panel_name": "Ciliary Dyskinesia",
"panel_id": 82,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ccdc103 has been classified as Green List (High Evidence).",
"entity_name": "CCDC103",
"entity_type": "gene"
},
{
"created": "2020-10-17T10:36:33.925882+11:00",
"panel_name": "Ciliary Dyskinesia",
"panel_id": 82,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CCDC103 were changed from to Ciliary dyskinesia, primary, 17, MIM# 614679",
"entity_name": "CCDC103",
"entity_type": "gene"
},
{
"created": "2020-10-17T10:36:06.180727+11:00",
"panel_name": "Ciliary Dyskinesia",
"panel_id": 82,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CCDC103 were set to ",
"entity_name": "CCDC103",
"entity_type": "gene"
},
{
"created": "2020-10-17T10:35:37.746246+11:00",
"panel_name": "Ciliary Dyskinesia",
"panel_id": 82,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CCDC103 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CCDC103",
"entity_type": "gene"
},
{
"created": "2020-10-17T10:35:09.135906+11:00",
"panel_name": "Ciliary Dyskinesia",
"panel_id": 82,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CCDC103: Rating: GREEN; Mode of pathogenicity: None; Publications: 22581229, 32447765, 31858719, 28790179; Phenotypes: Ciliary dyskinesia, primary, 17, MIM# 614679; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CCDC103",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:18:21.758253+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AARS2 as ready",
"entity_name": "AARS2",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:18:21.750586+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: aars2 has been classified as Green List (High Evidence).",
"entity_name": "AARS2",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:16:42.967678+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4976",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GARS as ready",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:16:42.957491+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4976",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gars has been classified as Green List (High Evidence).",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:16:32.727416+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4976",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GARS were changed from to Spinal muscular atrophy, infantile, James type, MIM# 619042; Charcot-Marie-Tooth disease, type 2D, MIM# 601472; Neuronopathy, distal hereditary motor, type VA, MIM# 600794; Multi-system mitochondrial disorder",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:16:09.133016+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4975",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GARS were set to ",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:15:49.249054+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4974",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GARS was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:15:30.282012+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4973",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: GARS.",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:15:14.840448+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4973",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GARS: Rating: GREEN; Mode of pathogenicity: None; Publications: 17101916, 22462675, 31985473, 32181591, 12690580, 25168514, 26503042, 29648643, 16982418, 24669931, 28594869; Phenotypes: Spinal muscular atrophy, infantile, James type, MIM# 619042, Charcot-Marie-Tooth disease, type 2D, MIM# 601472, Neuronopathy, distal hereditary motor, type VA, MIM# 600794, Multi-system mitochondrial disorder; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:14:10.699091+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GARS as ready",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:14:10.694484+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: New HGNC approved name is GARS1.",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:14:10.668909+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gars has been classified as Green List (High Evidence).",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:14:05.683782+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag new gene name tag was added to gene: GARS.",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:13:46.613059+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GARS were changed from to Spinal muscular atrophy, infantile, James type, MIM# 619042; Charcot-Marie-Tooth disease, type 2D, MIM# 601472; Neuronopathy, distal hereditary motor, type VA, MIM# 600794; Multi-system mitochondrial disorder",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:13:16.737169+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.515",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GARS were set to ",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:12:45.559886+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GARS was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-17T08:12:15.540171+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.513",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GARS: Rating: GREEN; Mode of pathogenicity: None; Publications: 17101916, 22462675, 31985473, 32181591, 12690580, 25168514, 26503042, 29648643, 16982418, 24669931, 28594869; Phenotypes: Spinal muscular atrophy, infantile, James type, MIM# 619042, Charcot-Marie-Tooth disease, type 2D, MIM# 601472, Neuronopathy, distal hereditary motor, type VA, MIM# 600794, Multi-system mitochondrial disorder; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "GARS",
"entity_type": "gene"
},
{
"created": "2020-10-16T21:06:19.166428+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4973",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SELENON as ready",
"entity_name": "SELENON",
"entity_type": "gene"
},
{
"created": "2020-10-16T21:06:19.155523+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4973",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: selenon has been classified as Green List (High Evidence).",
"entity_name": "SELENON",
"entity_type": "gene"
},
{
"created": "2020-10-16T21:06:09.680063+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4973",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SELENON were changed from to Myopathy, congenital, with fiber-type disproportion, MIM# 255310; Muscular dystrophy, rigid spine, 1, MIM# 602771",
"entity_name": "SELENON",
"entity_type": "gene"
},
{
"created": "2020-10-16T21:05:52.078043+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4972",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SELENON were set to ",
"entity_name": "SELENON",
"entity_type": "gene"
},
{
"created": "2020-10-16T21:05:35.517724+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4971",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SELENON was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "SELENON",
"entity_type": "gene"
},
{
"created": "2020-10-16T21:05:17.893931+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SELENON: Rating: GREEN; Mode of pathogenicity: None; Publications: 11528383, 12192640, 16365872, 21131290, 21131290, 32154989, 32796131; Phenotypes: Myopathy, congenital, with fiber-type disproportion, MIM# 255310, Muscular dystrophy, rigid spine, 1, MIM# 602771; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "SELENON",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:54:41.749743+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNNT1 as ready",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:54:41.737745+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnnt1 has been classified as Green List (High Evidence).",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:54:37.256122+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNNT1 were changed from to Nemaline myopathy 5, Amish type, MIM# 605355",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:54:07.947094+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.237",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNNT1 were set to ",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:53:40.836626+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.236",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNNT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:53:11.652089+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNNT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10952871, 32994279, 32819427, 31970803, 31604653, 29931346, 31680123; Phenotypes: Nemaline myopathy 5, Amish type, MIM# 605355; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:52:04.393705+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNNT1 as ready",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:52:04.386375+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnnt1 has been classified as Green List (High Evidence).",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:51:56.972024+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4970",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNNT1 were changed from to Nemaline myopathy 5, Amish type, MIM# 605355",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:51:28.480289+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4969",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNNT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:51:06.002523+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4968",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNNT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10952871, 32994279, 32819427, 31970803, 31604653, 29931346, 29178646; Phenotypes: Nemaline myopathy 5, Amish type, MIM# 605355; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TNNT1",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:45:31.332843+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNNT3 as ready",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:45:31.322030+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnnt3 has been classified as Green List (High Evidence).",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:45:28.707383+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNNT3 were changed from to Arthrogryposis, distal, type 2B2, MIM# 618435",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:45:01.716228+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.234",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNNT3 were set to ",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:44:30.495286+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: TNNT3 was changed from to Other",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:43:27.518194+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNNT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:42:57.905323+11:00",
"panel_name": "Arthrogryposis",
"panel_id": 47,
"panel_version": "0.231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNNT3: Rating: GREEN; Mode of pathogenicity: Other; Publications: 12865991, 19142688, 21402185, 25337069, 17194691; Phenotypes: Arthrogryposis, distal, type 2B2, MIM# 618435; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:42:15.569918+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4968",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TNNT3 as ready",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:42:15.559315+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4968",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tnnt3 has been classified as Green List (High Evidence).",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:42:08.790408+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4968",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TNNT3 were changed from to Arthrogryposis, distal, type 2B2, MIM# 618435",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:41:50.887657+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4967",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TNNT3 were set to ",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:41:32.909013+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4966",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: TNNT3 was changed from to Other",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:41:16.227261+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4965",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TNNT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:40:57.762768+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TNNT3: Rating: GREEN; Mode of pathogenicity: Other; Publications: 12865991, 19142688, 21402185, 25337069, 17194691; Phenotypes: Arthrogryposis, distal, type 2B2, MIM# 618435; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TNNT3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:35:03.888815+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STAC3 as ready",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:35:03.881409+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stac3 has been classified as Green List (High Evidence).",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:35:00.247035+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STAC3 were changed from Myopathy, Native American to Myopathy, congenital, Baily-Bloch, MIM# 255995",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:34:48.572936+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STAC3 were set to ",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:34:37.025221+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: STAC3 as Green List (high evidence)",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:34:37.014891+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stac3 has been classified as Green List (High Evidence).",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:34:24.452360+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: STAC3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23736855, 28411587, 28777491, 30168660; Phenotypes: Myopathy, congenital, Baily-Bloch, MIM# 255995; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:33:10.097667+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STAC3 as ready",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:33:10.086160+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stac3 has been classified as Green List (High Evidence).",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:33:01.956135+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: STAC3.",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:32:50.467338+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4964",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STAC3 were changed from to Myopathy, congenital, Baily-Bloch, MIM# 255995",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:32:33.117297+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4963",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STAC3 were set to ",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:32:06.321288+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: STAC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:31:47.704057+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: STAC3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23736855, 28411587, 28777491, 30168660; Phenotypes: Myopathy, congenital, Baily-Bloch, MIM# 255995; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:14:09.443021+11:00",
"panel_name": "Mackenzie's Mission_Reproductive Carrier Screening",
"panel_id": 3139,
"panel_version": "0.32",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SPEG was added\ngene: SPEG was added to Mackenzie's Mission_Reproductive Carrier Screening. Sources: Expert Review\nMode of inheritance for gene: SPEG was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SPEG were set to 25087613; 31625632; 30412272; 30157964; 29614691; 29474540; 28624463; 26578207; 25087613\nPhenotypes for gene: SPEG were set to Centronuclear myopathy 5, MIM# 615959\nReview for gene: SPEG was set to GREEN\nAdded comment: Centronuclear myopathy-5 is an autosomal recessive congenital myopathy characterized by severe neonatal hypotonia with respiratory insufficiency and difficulty feeding. Some individuals die in infancy, and some develop dilated cardiomyopathy. More than 10 unrelated families reported, functional data. \nSources: Expert Review",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:12:46.040955+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPEG as ready",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:12:46.030429+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: speg has been classified as Green List (High Evidence).",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:12:42.706822+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SPEG were changed from Centronuclear myopathy with dilated cardiomyopathy to Centronuclear myopathy 5, MIM# 615959",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:12:17.347296+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SPEG were set to ",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:11:54.666660+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SPEG as Green List (high evidence)",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:11:54.655866+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: speg has been classified as Green List (High Evidence).",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:11:42.601041+11:00",
"panel_name": "Additional findings_Paediatric",
"panel_id": 3302,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SPEG: Rating: GREEN; Mode of pathogenicity: None; Publications: 25087613, 31625632, 30412272, 30157964, 29614691, 29474540, 28624463, 26578207, 25087613; Phenotypes: Centronuclear myopathy 5, MIM# 615959; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:10:56.929258+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPEG as ready",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:10:56.921062+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: speg has been classified as Green List (High Evidence).",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:10:50.350219+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SPEG were changed from to Centronuclear myopathy 5, MIM# 615959",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:10:32.326582+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SPEG were set to ",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:10:13.285804+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4959",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SPEG was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T20:09:51.114739+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SPEG: Rating: GREEN; Mode of pathogenicity: None; Publications: 25087613, 31625632, 30412272, 30157964, 29614691, 29474540, 28624463, 26578207, 25087613; Phenotypes: Centronuclear myopathy 5, MIM# 615959; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2020-10-16T19:58:08.144168+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TPM3 as ready",
"entity_name": "TPM3",
"entity_type": "gene"
},
{
"created": "2020-10-16T19:58:08.132777+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tpm3 has been classified as Green List (High Evidence).",
"entity_name": "TPM3",
"entity_type": "gene"
},
{
"created": "2020-10-16T19:57:57.624405+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TPM3 were changed from to CAP myopathy 1, MIM# 609284; Myopathy, congenital, with fiber-type disproportion, MIM# 255310; Nemaline myopathy 1, autosomal dominant or recessive, MIM# 609284; Congenital muscle stiffness",
"entity_name": "TPM3",
"entity_type": "gene"
},
{
"created": "2020-10-16T19:57:39.223336+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4957",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TPM3 were set to ",
"entity_name": "TPM3",
"entity_type": "gene"
},
{
"created": "2020-10-16T19:57:20.767556+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4956",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: TPM3 was changed from to Other",
"entity_name": "TPM3",
"entity_type": "gene"
},
{
"created": "2020-10-16T19:57:02.422475+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4955",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TPM3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "TPM3",
"entity_type": "gene"
},
{
"created": "2020-10-16T19:56:39.877792+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4954",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TPM3: Rating: GREEN; Mode of pathogenicity: Other; Publications: 26418456, 7704029, 17376686, 18382475, 19487656; Phenotypes: CAP myopathy 1, MIM# 609284, Myopathy, congenital, with fiber-type disproportion, MIM# 255310, Nemaline myopathy 1, autosomal dominant or recessive, MIM# 609284, Congenital muscle stiffness; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "TPM3",
"entity_type": "gene"
},
{
"created": "2020-10-16T18:58:19.311072+11:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.513",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: MICU1.",
"entity_name": "MICU1",
"entity_type": "gene"
},
{
"created": "2020-10-16T18:57:55.551116+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.4954",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: MICU1.",
"entity_name": "MICU1",
"entity_type": "gene"
},
{
"created": "2020-10-16T18:57:37.245177+11:00",
"panel_name": "Muscular dystrophy_Paediatric",
"panel_id": 141,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MICU1 as ready",
"entity_name": "MICU1",
"entity_type": "gene"
},
{
"created": "2020-10-16T18:57:37.219940+11:00",
"panel_name": "Muscular dystrophy_Paediatric",
"panel_id": 141,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: micu1 has been classified as Green List (High Evidence).",
"entity_name": "MICU1",
"entity_type": "gene"
},
{
"created": "2020-10-16T18:57:29.918685+11:00",
"panel_name": "Muscular dystrophy_Paediatric",
"panel_id": 141,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MICU1 were changed from to Myopathy with extrapyramidal signs, MIM# 615673",
"entity_name": "MICU1",
"entity_type": "gene"
},
{
"created": "2020-10-16T18:57:03.103315+11:00",
"panel_name": "Muscular dystrophy_Paediatric",
"panel_id": 141,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag founder tag was added to gene: MICU1.",
"entity_name": "MICU1",
"entity_type": "gene"
},
{
"created": "2020-10-16T18:56:55.461712+11:00",
"panel_name": "Muscular dystrophy_Paediatric",
"panel_id": 141,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MICU1 were set to ",
"entity_name": "MICU1",
"entity_type": "gene"
},
{
"created": "2020-10-16T18:56:28.332356+11:00",
"panel_name": "Muscular dystrophy_Paediatric",
"panel_id": 141,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MICU1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MICU1",
"entity_type": "gene"
}
]
}