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"count": 221272,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=227",
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"results": [
{
"created": "2025-05-09T16:52:38.655139+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.839",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PQBP1 were changed from Renpenning syndrome, 309500 (3) to Renpenning syndrome MIM#309500",
"entity_name": "PQBP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:52:30.436202+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.838",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PQBP1 were set to ",
"entity_name": "PQBP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:52:01.767720+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.837",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PPT1 as ready",
"entity_name": "PPT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:52:01.760127+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.837",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ppt1 has been classified as Green List (High Evidence).",
"entity_name": "PPT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:51:59.783029+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.837",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PPT1 were changed from Ceroid lipofuscinosis, neuronal, 1, 256730 (3) to Ceroid lipofuscinosis, neuronal, 1, MIM# 256730",
"entity_name": "PPT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:51:50.518547+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.836",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PPT1 were set to ",
"entity_name": "PPT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:51:27.685678+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POU1F1 as ready",
"entity_name": "POU1F1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:51:27.675040+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pou1f1 has been classified as Green List (High Evidence).",
"entity_name": "POU1F1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:51:25.492449+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.835",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: POU1F1 were changed from Pituitary hormone deficiency, combined, 1, 613038 (3) to Pituitary hormone deficiency, combined or isolated, 1, MIM#613038",
"entity_name": "POU1F1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:51:16.251653+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.834",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: POU1F1 were set to ",
"entity_name": "POU1F1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:50:55.416632+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.833",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POR as ready",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:50:55.407147+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.833",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: por has been classified as Green List (High Evidence).",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:50:53.134026+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.833",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: POR were changed from Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, 201750 (3) to Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis (MIM#201750)",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:50:41.624232+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.832",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: POR were set to ",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:50:22.795581+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.831",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POMT2 as ready",
"entity_name": "POMT2",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:50:22.788155+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.831",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pomt2 has been classified as Green List (High Evidence).",
"entity_name": "POMT2",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:50:20.348818+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.831",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: POMT2 were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2, 613150 (3) to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2, MIM# 613150; Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2, MIM# 613156",
"entity_name": "POMT2",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:50:09.073730+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.830",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: POMT2 were set to ",
"entity_name": "POMT2",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:49:46.392574+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POMT1 as ready",
"entity_name": "POMT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:49:46.375674+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pomt1 has been classified as Green List (High Evidence).",
"entity_name": "POMT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:49:43.816155+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.829",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: POMT1 were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1, 236670 (3) to Myopathy caused by variation in POMT1 MONDO:0700070",
"entity_name": "POMT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:49:33.086420+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.828",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: POMT1 were set to ",
"entity_name": "POMT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:49:14.863951+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.827",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POMGNT1 as ready",
"entity_name": "POMGNT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:49:14.857054+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.827",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pomgnt1 has been classified as Green List (High Evidence).",
"entity_name": "POMGNT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:49:12.219966+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.827",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: POMGNT1 were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3, 253280 (3) to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3, MIM#253280; Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B3, MIM#61315",
"entity_name": "POMGNT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:48:37.666699+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.826",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: POMGNT1 were set to ",
"entity_name": "POMGNT1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:48:08.346529+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POLR3B as ready",
"entity_name": "POLR3B",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:48:08.339609+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: polr3b has been classified as Green List (High Evidence).",
"entity_name": "POLR3B",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:48:06.256181+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.825",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: POLR3B were changed from Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism, 614381 (3) to Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism,MIM#614381",
"entity_name": "POLR3B",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:47:55.394765+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.824",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: POLR3B were set to ",
"entity_name": "POLR3B",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:47:34.467851+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.823",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POLR1C as ready",
"entity_name": "POLR1C",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:47:34.460720+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.823",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: polr1c has been classified as Green List (High Evidence).",
"entity_name": "POLR1C",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:47:32.580053+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.823",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: POLR1C were changed from Treacher Collins syndrome 3, 248390 (3) to Leukodystrophy, hypomyelinating, 11 MIM#616494; Treacher Collins syndrome 3 MIM#248390",
"entity_name": "POLR1C",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:47:15.184972+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.822",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: POLR1C were set to ",
"entity_name": "POLR1C",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:46:49.340622+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POLG as ready",
"entity_name": "POLG",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:46:49.329985+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: polg has been classified as Green List (High Evidence).",
"entity_name": "POLG",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:46:47.299569+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: POLG were changed from Mitochondrial DNA depletion syndrome 4A (Alpers type), 203700 (3) to Mitochondrial DNA depletion syndrome 4A (Alpers type), MIM# 203700; Mitochondrial DNA depletion syndrome 4B (MNGIE type), MIM#613662",
"entity_name": "POLG",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:46:25.020336+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.820",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PNPO as ready",
"entity_name": "PNPO",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:46:25.012833+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.820",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pnpo has been classified as Green List (High Evidence).",
"entity_name": "PNPO",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:46:23.079428+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.820",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PNPO were changed from Pyridoxamine 5'-phosphate oxidase deficiency, 610090 (3) to Pyridoxamine 5'-phosphate oxidase deficiency MIM#610090",
"entity_name": "PNPO",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:46:14.295296+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.819",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PNPO were set to ",
"entity_name": "PNPO",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:45:22.729751+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.818",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PNKP as ready",
"entity_name": "PNKP",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:45:22.722794+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.818",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pnkp has been classified as Green List (High Evidence).",
"entity_name": "PNKP",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:45:20.796368+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.818",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PNKP were changed from Microcephaly, seizures, and developmental delay, 613402 (3) to Ataxia-oculomotor apraxia 4, MIM# 616267; Microcephaly, seizures, and developmental delay, MIM# 613402",
"entity_name": "PNKP",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:44:56.107052+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.817",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PNKP were set to ",
"entity_name": "PNKP",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:44:35.721844+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PMM2 as ready",
"entity_name": "PMM2",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:44:35.715564+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pmm2 has been classified as Green List (High Evidence).",
"entity_name": "PMM2",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:44:33.816443+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PMM2 were changed from Congenital disorder of glycosylation, type Ia, 212065 (3) to Congenital disorder of glycosylation, type Ia (MIM#212065)",
"entity_name": "PMM2",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:44:11.340406+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.815",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PLPBP as ready",
"entity_name": "PLPBP",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:44:11.330834+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.815",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: plpbp has been classified as Green List (High Evidence).",
"entity_name": "PLPBP",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:44:09.230854+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.815",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PLPBP were changed from Epilepsy, early-onset, vitamin B6-dependent, 617290 (3), Autosomal recessive to Epilepsy, early-onset, vitamin B6-dependent, MIM#617290",
"entity_name": "PLPBP",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:43:59.551640+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.814",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PLPBP were set to ",
"entity_name": "PLPBP",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:43:03.503409+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PLP1 as ready",
"entity_name": "PLP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:43:03.493458+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: plp1 has been classified as Green List (High Evidence).",
"entity_name": "PLP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:43:00.883761+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PLP1 were changed from Pelizaeus-Merzbacher disease, 312080 (3) to Pelizaeus-Merzbacher disease MIM#312080, Pelizeaus-Merzbacher spectrum disorder MONDO:0010714; Spastic paraplegia 2, X-linked MIM#312920, hereditary spastic paraplegia 2 MONDO:0010733",
"entity_name": "PLP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:42:45.204306+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.812",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PLP1 were set to ",
"entity_name": "PLP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:42:25.861084+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.811",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PLOD1 as ready",
"entity_name": "PLOD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:42:25.851336+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.811",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: plod1 has been classified as Green List (High Evidence).",
"entity_name": "PLOD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:42:23.662466+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.811",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PLOD1 were changed from Ehlers-Danlos syndrome, type VI, 225400 (3) to Ehlers-Danlos syndrome, kyphoscoliotic type, 1, MIM# 225400",
"entity_name": "PLOD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:42:13.768560+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.810",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PLOD1 were set to ",
"entity_name": "PLOD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:41:52.646772+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.809",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PLA2G6 as ready",
"entity_name": "PLA2G6",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:41:52.639669+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.809",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pla2g6 has been classified as Green List (High Evidence).",
"entity_name": "PLA2G6",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:41:38.201137+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.809",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PKHD1 as ready",
"entity_name": "PKHD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:41:38.194651+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.809",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pkhd1 has been classified as Green List (High Evidence).",
"entity_name": "PKHD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:41:07.159746+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.809",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PKHD1 were changed from Polycystic kidney and hepatic disease, 263200 (3) to Polycystic kidney disease 4, with or without hepatic disease MIM#263200",
"entity_name": "PKHD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:40:56.934966+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.808",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PKHD1 were set to ",
"entity_name": "PKHD1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:40:31.013065+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.807",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGT as ready",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:40:31.003391+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.807",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigt has been classified as Green List (High Evidence).",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:40:28.864471+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.807",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGT were changed from Multiple congenital anomalies-hypotonia-seizures syndrome 3 to Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM# 615398, MONDO:0014165",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:40:17.155346+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.806",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGT were set to ",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:39:55.350167+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.805",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGN as ready",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:39:55.340410+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.805",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pign has been classified as Green List (High Evidence).",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:39:53.400226+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.805",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGN were changed from Multiple congenital anomalies-hypotonia-seizures syndrome 1, 614080 (3) to Multiple congenital anomalies-hypotonia-seizures syndrome 1,MIM#614080",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:39:42.295036+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.804",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGN were set to ",
"entity_name": "PIGN",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:39:21.116063+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.803",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGG as ready",
"entity_name": "PIGG",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:39:21.100402+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.803",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigg has been classified as Green List (High Evidence).",
"entity_name": "PIGG",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:39:01.902065+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.803",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGG were set to ",
"entity_name": "PIGG",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:38:43.761503+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIBF1 as ready",
"entity_name": "PIBF1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:38:43.750457+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pibf1 has been classified as Green List (High Evidence).",
"entity_name": "PIBF1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:38:28.981400+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PHYH as ready",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:38:28.970497+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: phyh has been classified as Green List (High Evidence).",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:38:17.055961+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PHYH were changed from Refsum disease, 266500 (3) to Refsum disease MIM#266500",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:38:07.321716+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.801",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PHYH were set to ",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:37:39.385580+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.800",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PHGDH as ready",
"entity_name": "PHGDH",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:37:39.370101+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.800",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: phgdh has been classified as Green List (High Evidence).",
"entity_name": "PHGDH",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:37:36.669686+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.800",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PHGDH were changed from Neu-Laxova syndrome1, 256520 (3) to Neu-Laxova syndrome 1 MIM#256520; Phosphoglycerate dehydrogenase deficiency MIM#601815",
"entity_name": "PHGDH",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:37:28.722288+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.799",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PHGDH were set to ",
"entity_name": "PHGDH",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:37:07.087626+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PHF8 as ready",
"entity_name": "PHF8",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:37:07.080334+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: phf8 has been classified as Green List (High Evidence).",
"entity_name": "PHF8",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:37:05.159132+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PHF8 were changed from Mental retardation syndrome, X-linked, Siderius type, 300263 (3) to Intellectual developmental disorder, X-linked syndromic, Siderius type, MIM#\t300263",
"entity_name": "PHF8",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:36:37.518529+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.797",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PHF8 were set to ",
"entity_name": "PHF8",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:36:16.090784+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.796",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGM3 as ready",
"entity_name": "PGM3",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:36:16.083798+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.796",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgm3 has been classified as Green List (High Evidence).",
"entity_name": "PGM3",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:36:13.902277+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.796",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PGM3 were changed from Immunodeficiency 23, 615816 (3) to Immunodeficiency 23, MIM# 615816",
"entity_name": "PGM3",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:36:05.685489+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.795",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PGM3 were set to ",
"entity_name": "PGM3",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:35:45.634570+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGM1 as ready",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:35:45.626861+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgm1 has been classified as Green List (High Evidence).",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:35:43.895176+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PGM1 were changed from Congenital disorder of glycosylation, type It, 614921 (3) to Congenital disorder of glycosylation, type It (MIM#614921)",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:35:34.294229+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.793",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PGM1 were set to ",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T16:35:14.902485+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.792",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGK1 as ready",
"entity_name": "PGK1",
"entity_type": "gene"
}
]
}