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{
"count": 221277,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=229",
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"results": [
{
"created": "2025-05-09T15:55:21.251544+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PAH were changed from Phenylketonuria, 261600 (3) to Phenylketonuria,MIM#261600",
"entity_name": "PAH",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:55:12.225236+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PAH were set to ",
"entity_name": "PAH",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:54:50.163780+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: P3H1 as ready",
"entity_name": "P3H1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:54:50.157293+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: p3h1 has been classified as Green List (High Evidence).",
"entity_name": "P3H1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:54:47.942608+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: P3H1 were changed from Osteogenesis imperfecta, type VIII, 610915 (3) to Osteogenesis imperfecta, type VIII, MIM#610915",
"entity_name": "P3H1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:54:39.206591+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.746",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: P3H1 were set to ",
"entity_name": "P3H1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:36:05.265484+10:00",
"panel_name": "Genomic newborn screening: BabyScreen+",
"panel_id": 3931,
"panel_version": "1.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRPM4 were changed from Progressive familial heart block, type IB 604559 to Progressive familial heart block, type IB, MIM# 604559",
"entity_name": "TRPM4",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:35:51.069479+10:00",
"panel_name": "Genomic newborn screening: BabyScreen+",
"panel_id": 3931,
"panel_version": "1.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRPM4 as Red List (low evidence)",
"entity_name": "TRPM4",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:35:51.060840+10:00",
"panel_name": "Genomic newborn screening: BabyScreen+",
"panel_id": 3931,
"panel_version": "1.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trpm4 has been classified as Red List (Low Evidence).",
"entity_name": "TRPM4",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:35:41.351797+10:00",
"panel_name": "Genomic newborn screening: BabyScreen+",
"panel_id": 3931,
"panel_version": "1.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRPM4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Progressive familial heart block, type IB, MIM# 604559; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRPM4",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:27:47.229766+10:00",
"panel_name": "Genomic newborn screening: BabyScreen+",
"panel_id": 3931,
"panel_version": "1.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCNE2 as ready",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:27:47.219998+10:00",
"panel_name": "Genomic newborn screening: BabyScreen+",
"panel_id": 3931,
"panel_version": "1.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:27:44.471750+10:00",
"panel_name": "Genomic newborn screening: BabyScreen+",
"panel_id": 3931,
"panel_version": "1.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KCNE2 were changed from Long QT syndrome-6 to Long QT syndrome 6, MIM# 613693",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:27:33.544338+10:00",
"panel_name": "Genomic newborn screening: BabyScreen+",
"panel_id": 3931,
"panel_version": "1.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KCNE2 as Red List (low evidence)",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:27:33.537737+10:00",
"panel_name": "Genomic newborn screening: BabyScreen+",
"panel_id": 3931,
"panel_version": "1.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcne2 has been classified as Red List (Low Evidence).",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:27:24.105506+10:00",
"panel_name": "Genomic newborn screening: BabyScreen+",
"panel_id": 3931,
"panel_version": "1.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: KCNE2: Changed phenotypes: Long QT syndrome 6, MIM# 613693",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:27:10.906671+10:00",
"panel_name": "Genomic newborn screening: BabyScreen+",
"panel_id": 3931,
"panel_version": "1.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: KCNE2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KCNE2",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:17:00.634824+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OTC as ready",
"entity_name": "OTC",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:17:00.624518+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: otc has been classified as Green List (High Evidence).",
"entity_name": "OTC",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:16:58.449528+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OTC were changed from Ornithine transcarbamylase deficiency, 311250 (3) to Ornithine transcarbamylase deficiency, MIM# 311250",
"entity_name": "OTC",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:16:49.509107+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OTC were set to ",
"entity_name": "OTC",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:16:09.850758+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OSTM1 as ready",
"entity_name": "OSTM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:16:09.839631+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ostm1 has been classified as Green List (High Evidence).",
"entity_name": "OSTM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:16:07.201120+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OSTM1 were changed from Osteopetrosis, autosomal recessive 5, 259720 (3) to Osteopetrosis, autosomal recessive 5, MIM#259720",
"entity_name": "OSTM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:15:57.599900+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OSTM1 were set to ",
"entity_name": "OSTM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:15:19.466265+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OPHN1 as ready",
"entity_name": "OPHN1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:15:19.459085+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ophn1 has been classified as Green List (High Evidence).",
"entity_name": "OPHN1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:15:16.889901+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OPHN1 were changed from Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance, 300486 (3) to Intellectual developmental disorder, X-linked syndromic, Billuart type MIM#300486; X-linked intellectual disability-cerebellar hypoplasia syndrome MONDO:0010337",
"entity_name": "OPHN1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:15:06.682822+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OPHN1 were set to ",
"entity_name": "OPHN1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:14:44.100676+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.739",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OPA3 as ready",
"entity_name": "OPA3",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:14:44.093689+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.739",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: opa3 has been classified as Green List (High Evidence).",
"entity_name": "OPA3",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:14:42.431503+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.739",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OPA3 were changed from 3-methylglutaconic aciduria, type III, 258501 (3) to 3-methylglutaconic aciduria, type III MIM#258501; 3-methylglutaconic aciduria type 3 MONDO:0009787",
"entity_name": "OPA3",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:14:32.401822+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OPA3 were set to ",
"entity_name": "OPA3",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:14:11.787650+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.737",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OPA1 as ready",
"entity_name": "OPA1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:14:11.780710+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.737",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: opa1 has been classified as Green List (High Evidence).",
"entity_name": "OPA1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:14:09.397027+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.737",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OPA1 were changed from Behr syndrome, 210000 (3), Autosomal recessive to Behr syndrome, MIM#210000",
"entity_name": "OPA1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:13:53.468444+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OPA1 were set to ",
"entity_name": "OPA1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:13:36.046450+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OFD1 as ready",
"entity_name": "OFD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:13:36.039776+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ofd1 has been classified as Green List (High Evidence).",
"entity_name": "OFD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:13:34.021527+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OFD1 were changed from Joubert syndrome 10, 300804 (3) to Joubert syndrome 10 MIM#300804; Simpson-Golabi-Behmel syndrome, type 2 MIM#300209; Retinitis pigmentosa 23 MIM#300424",
"entity_name": "OFD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:13:24.662037+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.734",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OFD1 were set to ",
"entity_name": "OFD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:13:01.359388+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OCRL as ready",
"entity_name": "OCRL",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:13:01.353001+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ocrl has been classified as Green List (High Evidence).",
"entity_name": "OCRL",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:12:59.253880+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OCRL were changed from Lowe syndrome, 309000 (3) to Dent disease 2 MIM#300555; Lowe syndrome MIM#309000",
"entity_name": "OCRL",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:12:48.735888+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.732",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OCRL were set to ",
"entity_name": "OCRL",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:12:20.604777+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.731",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NTRK1 as ready",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:12:20.595095+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.731",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ntrk1 has been classified as Green List (High Evidence).",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:12:18.391297+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.731",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NTRK1 were changed from Insensitivity to pain, congenital, with anhidrosis, 256800 (3) to Insensitivity to pain, congenital, with anhidrosis MIM#256800",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:12:07.965308+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.730",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NTRK1 were set to ",
"entity_name": "NTRK1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:11:48.435486+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.729",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NR0B1 as ready",
"entity_name": "NR0B1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:11:48.425110+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.729",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nr0b1 has been classified as Green List (High Evidence).",
"entity_name": "NR0B1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:11:46.552752+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.729",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NR0B1 were changed from 46XY sex reversal 2, dosage-sensitive, 300018 (3) to Adrenal hypoplasia, congenital, MIM#300200",
"entity_name": "NR0B1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:11:36.142902+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.728",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NR0B1 were set to ",
"entity_name": "NR0B1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:11:15.738410+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.727",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NPHS2 as ready",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:11:15.731945+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.727",
"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": "2025-05-09T15:11:13.677567+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.727",
"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": "2025-05-09T15:11:03.854209+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.726",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NPHS2 were set to ",
"entity_name": "NPHS2",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:10:23.630214+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.725",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NPHS1 as ready",
"entity_name": "NPHS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:10:23.622970+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.725",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nphs1 has been classified as Green List (High Evidence).",
"entity_name": "NPHS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:10:21.380584+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.725",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NPHS1 were changed from Nephrotic syndrome, type 1, 256300 (3) to Nephrotic syndrome, type 1, MIM# 256300; congenital nephrotic syndrome, Finnish type MONDO:0009732",
"entity_name": "NPHS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:10:11.521768+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.724",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NPHS1 were set to ",
"entity_name": "NPHS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:09:53.007456+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.723",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NPHP3 as ready",
"entity_name": "NPHP3",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:09:52.999665+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.723",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nphp3 has been classified as Green List (High Evidence).",
"entity_name": "NPHP3",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:09:50.558286+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.723",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NPHP3 were changed from Meckel syndrome 7, 267010 (3) to Renal-hepatic-pancreatic dysplasia 1 MIM#208540; Meckel syndrome 7 MIM#267010; Nephronophthisis 3 MIM#604387",
"entity_name": "NPHP3",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:09:31.580226+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.722",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NPHP1 as ready",
"entity_name": "NPHP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:09:31.570682+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.722",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nphp1 has been classified as Green List (High Evidence).",
"entity_name": "NPHP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:09:29.504134+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.722",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NPHP1 were changed from Joubert syndrome 4, 609583 (3) to Nephronophthisis 1, juvenile MIM#256100; Joubert syndrome 4 MIM#609583; Senior-Loken syndrome-1 MIM#266900",
"entity_name": "NPHP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:09:09.221843+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.721",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NPC2 as ready",
"entity_name": "NPC2",
"entity_type": "gene"
},
{
"created": "2025-05-09T15:09:09.211483+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.721",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: npc2 has been classified as Green List (High Evidence).",
"entity_name": "NPC2",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:48:37.794746+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.721",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NPC1 as ready",
"entity_name": "NPC1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:48:37.787644+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.721",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: npc1 has been classified as Green List (High Evidence).",
"entity_name": "NPC1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:44:48.345295+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.721",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NPC1 were set to 11333381; 26910362",
"entity_name": "NPC1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:44:20.305544+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.720",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NNT as ready",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:44:20.295760+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.720",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nnt has been classified as Green List (High Evidence).",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:44:17.133571+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.720",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NNT were changed from Glucocorticoid deficiency 4, 614736 (3) to Glucocorticoid deficiency 4, with or without mineralocorticoid deficiency MIM#614736; MONDO:0013874",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:43:35.435768+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.719",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NNT were set to ",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:43:14.825299+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.718",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NGLY1 as ready",
"entity_name": "NGLY1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:43:14.815487+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.718",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ngly1 has been classified as Green List (High Evidence).",
"entity_name": "NGLY1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:43:10.303826+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.718",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NGLY1 were changed from Congenital disorder of deglycosylation, 615273 (3) to Congenital disorder of deglycosylation, MIM#615273",
"entity_name": "NGLY1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:42:43.649295+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.717",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NGLY1 were set to ",
"entity_name": "NGLY1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:42:19.718947+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.716",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEU1 as ready",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:42:19.708605+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.716",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neu1 has been classified as Green List (High Evidence).",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:42:16.630539+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.716",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEU1 were changed from Sialidosis, type I, 256550 (3) to Sialidosis, type I, MIM #256550; Sialidosis, type II, MIM #256550",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:42:06.348461+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.715",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEU1 were set to ",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:41:37.624656+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.714",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEB as ready",
"entity_name": "NEB",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:41:37.617929+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.714",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neb has been classified as Green List (High Evidence).",
"entity_name": "NEB",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:41:28.158493+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.714",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEB were set to 27228465",
"entity_name": "NEB",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:41:04.195021+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.713",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFV1 as ready",
"entity_name": "NDUFV1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:41:04.184966+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.713",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufv1 has been classified as Green List (High Evidence).",
"entity_name": "NDUFV1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:41:01.193209+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.713",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFV1 were changed from Mitochondrial complex I deficiency, 252010 (3) to Mitochondrial complex I deficiency, nuclear type 4 MIM#618225",
"entity_name": "NDUFV1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:40:51.600225+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.712",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFV1 were set to ",
"entity_name": "NDUFV1",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:40:16.534538+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS7 as ready",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:40:16.523731+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs7 has been classified as Green List (High Evidence).",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:40:10.468270+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.711",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS7 were changed from Leigh syndrome, 256000 (3) to Mitochondrial complex I deficiency, nuclear type 3 MIM#618224",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:40:00.489303+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.710",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFS7 were set to ",
"entity_name": "NDUFS7",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:39:40.666036+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.709",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS6 as ready",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:39:40.659050+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.709",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs6 has been classified as Green List (High Evidence).",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:39:38.449479+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.709",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS6 were changed from Mitochondrial complex I deficiency, 252010 (3) to Mitochondrial complex I deficiency, nuclear type 9 (MIM#618232)",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:39:28.861225+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.708",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFS6 were set to ",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2025-05-09T14:38:47.403270+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.707",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS4 as ready",
"entity_name": "NDUFS4",
"entity_type": "gene"
}
]
}