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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=282",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=280",
"results": [
{
"created": "2025-03-24T16:34:25.555785+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1685",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NT5C2 were set to ",
"entity_name": "NT5C2",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:33:55.509336+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NSUN2 as ready",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:33:55.502839+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nsun2 has been classified as Green List (High Evidence).",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:33:52.436370+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1684",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NSUN2 were changed from Mental retardation, autosomal recessive 5, 611091 (3) to Intellectual developmental disorder, autosomal recessive 5, MIM# 611091",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:33:40.572731+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1683",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NSUN2 were set to ",
"entity_name": "NSUN2",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:33:06.977677+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NPHS2 as ready",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:33:06.968002+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nphs2 has been classified as Green List (High Evidence).",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:33:01.386794+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1682",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NPHS2 were changed from Nephrotic syndrome, type 2, 600995 (3) to Nephrotic syndrome, type 2 MIM#600995",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:32:50.548548+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1681",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NPHS2 were set to ",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:32:01.100457+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NIPAL4 as ready",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:32:01.094008+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nipal4 has been classified as Green List (High Evidence).",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:31:54.671340+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1680",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NIPAL4 were changed from Ichthyosis, congenital, autosomal recessive 6, 612281 (3) to Ichthyosis, congenital, autosomal recessive 6 MIM#612281",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:31:42.640768+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1679",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NIPAL4 were set to ",
"entity_name": "NIPAL4",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:31:02.344274+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1678",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NHS as ready",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:31:02.333370+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1678",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nhs has been classified as Green List (High Evidence).",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:30:54.843167+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1678",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NHS were changed from Cataract 40, X-linked, 302200 (3) to Nance-Horan syndrome MIM#302350",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:30:45.318902+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1677",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NHS were set to ",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:30:30.584913+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1676",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NHS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Nance-Horan syndrome MIM#302350; Mode of inheritance: None",
"entity_name": "NHS",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:29:40.189934+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1676",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEK8 as ready",
"entity_name": "NEK8",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:29:40.180451+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1676",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nek8 has been classified as Green List (High Evidence).",
"entity_name": "NEK8",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:29:30.757006+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1676",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEK8 were changed from Renal-hepatic-pancreatic dysplasia 2, 615415 (3), Autosomal recessive to Renal-hepatic-pancreatic dysplasia 2 MIM#615415",
"entity_name": "NEK8",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:29:10.767343+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1675",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEK8 were set to ",
"entity_name": "NEK8",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:28:11.050405+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1674",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS1 as ready",
"entity_name": "NDUFS1",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:28:11.044457+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1674",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs1 has been classified as Green List (High Evidence).",
"entity_name": "NDUFS1",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:28:08.198534+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1674",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS1 were changed from Mitochondrial complex I deficiency, 252010 (3) to Mitochondrial complex I deficiency, nuclear type 5, MIM#618226",
"entity_name": "NDUFS1",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:27:56.095507+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFS1 were set to ",
"entity_name": "NDUFS1",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:27:18.458192+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NAXE as ready",
"entity_name": "NAXE",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:27:18.451973+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: naxe has been classified as Green List (High Evidence).",
"entity_name": "NAXE",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:27:15.133443+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NAXE were changed from Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 617186 (3), Autosomal recessive to Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, MIM #617186",
"entity_name": "NAXE",
"entity_type": "gene"
},
{
"created": "2025-03-24T16:26:56.868140+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NAXE were set to ",
"entity_name": "NAXE",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:15:55.726135+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPLKIP as ready",
"entity_name": "MPLKIP",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:15:55.716185+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mplkip has been classified as Green List (High Evidence).",
"entity_name": "MPLKIP",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:15:53.090008+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MPLKIP were changed from Trichothiodystrophy 4, nonphotosensitive, 234050 (3) to Trichothiodystrophy 4, nonphotosensitive MIM#234050",
"entity_name": "MPLKIP",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:15:42.320371+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MPLKIP were set to ",
"entity_name": "MPLKIP",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:14:51.549198+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MMAB as ready",
"entity_name": "MMAB",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:14:51.542481+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mmab has been classified as Green List (High Evidence).",
"entity_name": "MMAB",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:14:49.099221+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MMAB were changed from Methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type, 251110 (3) to Methylmalonic aciduria, vitamin B12-responsive, cblB type MIM#251110",
"entity_name": "MMAB",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:14:36.787557+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MMAB were set to ",
"entity_name": "MMAB",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:14:05.316578+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MGAT2 as ready",
"entity_name": "MGAT2",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:14:05.309767+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mgat2 has been classified as Green List (High Evidence).",
"entity_name": "MGAT2",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:14:01.885994+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MGAT2 were changed from Congenital disorder of glycosylation, type IIa, 212066 (3) to Congenital disorder of glycosylation, type IIa MIM#212066",
"entity_name": "MGAT2",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:13:51.565364+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1665",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MGAT2 were set to ",
"entity_name": "MGAT2",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:12:54.221256+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MCFD2 as ready",
"entity_name": "MCFD2",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:12:54.203052+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mcfd2 has been classified as Green List (High Evidence).",
"entity_name": "MCFD2",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:12:51.643025+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MCFD2 were changed from Factor V and factor VIII, combined deficiency of, 613625 (3) to Factor V and factor VIII, combined deficiency of MIM#613625",
"entity_name": "MCFD2",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:12:39.497383+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1663",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MCFD2 were set to ",
"entity_name": "MCFD2",
"entity_type": "gene"
},
{
"created": "2025-03-24T14:12:15.568316+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MCFD2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Factor V and factor VIII, combined deficiency of MIM#613625; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MCFD2",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:44:38.433908+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MALT1 as ready",
"entity_name": "MALT1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:44:38.427463+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: malt1 has been classified as Green List (High Evidence).",
"entity_name": "MALT1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:44:36.268874+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MALT1 were changed from Immunodeficiency 12, 615468 (3) to Immunodeficiency 12 MIM#615468",
"entity_name": "MALT1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:44:25.831980+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1661",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MALT1 were set to ",
"entity_name": "MALT1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:43:59.067472+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1660",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LTBP4 as ready",
"entity_name": "LTBP4",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:43:59.061192+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1660",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ltbp4 has been classified as Green List (High Evidence).",
"entity_name": "LTBP4",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:43:55.846828+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1660",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LTBP4 were changed from Cutis laxa, autosomal recessive, type IC, 613177 (3) to Cutis laxa, autosomal recessive, type IC, #613177",
"entity_name": "LTBP4",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:43:40.280635+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1659",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LTBP4 were set to ",
"entity_name": "LTBP4",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:43:15.368161+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LTBP3 as ready",
"entity_name": "LTBP3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:43:15.361445+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ltbp3 has been classified as Green List (High Evidence).",
"entity_name": "LTBP3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:43:13.066114+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LTBP3 were changed from Tooth agenesis, selective, 6, 613097 (3) to Dental anomalies and short stature, MIM #601216",
"entity_name": "LTBP3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:43:02.770508+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1657",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LTBP3 were set to ",
"entity_name": "LTBP3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:42:30.427943+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LRP5 as ready",
"entity_name": "LRP5",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:42:30.425372+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: Prepair only screens for recessive conditions.",
"entity_name": "LRP5",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:42:30.400045+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lrp5 has been classified as Green List (High Evidence).",
"entity_name": "LRP5",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:42:13.789735+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LRP5 were changed from Osteoporosis-pseudoglioma syndrome, 259770 (3) to Exudative vitreoretinopathy 4 MIM#601813; Osteoporosis-pseudoglioma syndrome MIM#259770",
"entity_name": "LRP5",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:41:48.641212+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1655",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LRP5 were set to ",
"entity_name": "LRP5",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:41:15.417889+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1654",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LRP2 as ready",
"entity_name": "LRP2",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:41:15.408057+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1654",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lrp2 has been classified as Green List (High Evidence).",
"entity_name": "LRP2",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:41:12.704659+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1654",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LRP2 were changed from Donnai-Barrow syndrome, 222448 (3) to Donnai-Barrow syndrome, MIM #222448",
"entity_name": "LRP2",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:41:02.119394+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1653",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LRP2 were set to ",
"entity_name": "LRP2",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:40:25.245296+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1652",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LRIG2 as ready",
"entity_name": "LRIG2",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:40:25.231030+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1652",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lrig2 has been classified as Green List (High Evidence).",
"entity_name": "LRIG2",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:40:22.401844+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1652",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LRIG2 were changed from Urofacial syndrome 2, 615112 (3) to Urofacial syndrome 2, MIM #615112",
"entity_name": "LRIG2",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:40:12.055844+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1651",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LRIG2 were set to ",
"entity_name": "LRIG2",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:39:31.872859+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1650",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LIPT1 as ready",
"entity_name": "LIPT1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:39:31.863122+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1650",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lipt1 has been classified as Green List (High Evidence).",
"entity_name": "LIPT1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:35:32.754700+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1650",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LIPT1 were changed from Lipoyltransferase 1 deficiency, 616299 (3) to Lipoyltransferase 1 deficiency, MIM#616299",
"entity_name": "LIPT1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:35:22.983973+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1649",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LIPT1 were set to ",
"entity_name": "LIPT1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:35:08.828309+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1648",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LIPT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 29681092; Phenotypes: Lipoyltransferase 1 deficiency, MIM#616299; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LIPT1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:31:24.519633+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1648",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAMB3 as ready",
"entity_name": "LAMB3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:31:24.512622+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1648",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lamb3 has been classified as Green List (High Evidence).",
"entity_name": "LAMB3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:31:21.350302+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1648",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LAMB3 were changed from Epidermolysis bullosa, junctional, Herlitz type, 226700 (3) to Epidermolysis bullosa, junctional 1A, intermediate MIM#226650; Epidermolysis bullosa, junctional 1B, severe MIM#226700",
"entity_name": "LAMB3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:31:10.920194+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1647",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAMB3 were set to ",
"entity_name": "LAMB3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:30:39.953372+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1646",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAMA3 as ready",
"entity_name": "LAMA3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:30:39.946965+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1646",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lama3 has been classified as Green List (High Evidence).",
"entity_name": "LAMA3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:30:36.772329+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1646",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LAMA3 were changed from Epidermolysis bullosa, junctional, Herlitz type, 226700 (3) to Epidermolysis bullosa, junctional 2B, severe (MIM#619784); 3. Epidermolysis bullosa, junctional 2C, laryngoonychocutaneous (MIM#245660); Epidermolysis bullosa, junctional 2A, intermediate (MIM#619783)",
"entity_name": "LAMA3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:30:22.198556+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1645",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAMA3 were set to ",
"entity_name": "LAMA3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:29:56.428901+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1644",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAMA1 as ready",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:29:56.422442+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1644",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lama1 has been classified as Green List (High Evidence).",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:29:53.412579+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1644",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LAMA1 were changed from Poretti-Boltshauser syndrome, 615960 (3) to Poretti-Boltshauser syndrome, MIM #615960",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:29:42.849823+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1643",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAMA1 were set to ",
"entity_name": "LAMA1",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:29:11.615634+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1642",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KLHL40 as ready",
"entity_name": "KLHL40",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:29:11.609365+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1642",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: klhl40 has been classified as Green List (High Evidence).",
"entity_name": "KLHL40",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:29:08.983539+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1642",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KLHL40 were changed from Nemaline myopathy 8, autosomal recessive, 615348 (3) to Nemaline myopathy 8, autosomal recessive MIM#615348",
"entity_name": "KLHL40",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:28:57.985395+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1641",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KLHL40 were set to ",
"entity_name": "KLHL40",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:28:22.664833+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1640",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: JAM3 as ready",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:28:22.654041+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1640",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jam3 has been classified as Green List (High Evidence).",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:28:20.379929+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1640",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: JAM3 were changed from Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, 613730 (3) to Haemorrhagic destruction of the brain, subependymal calcification, and cataracts MIM#613730",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:28:03.015611+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1639",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: JAM3 were set to ",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:27:36.206827+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1638",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IVD as ready",
"entity_name": "IVD",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:27:36.200413+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1638",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ivd has been classified as Green List (High Evidence).",
"entity_name": "IVD",
"entity_type": "gene"
},
{
"created": "2025-03-24T13:27:32.975882+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1638",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IVD were changed from Isovaleric acidemia, 243500 (3) to Isovaleric acidemia, MIM #243500",
"entity_name": "IVD",
"entity_type": "gene"
}
]
}