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"count": 221277,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=231",
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"results": [
{
"created": "2025-05-09T13:57:53.766955+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.660",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MPV17 were changed from Mitochondrial DNA depletion syndrome 6 (hepatocerebral type), 256810 (3) to Charcot-Marie-Tooth disease, axonal, type 2EE, MIM#618400; Mitochondrial DNA depletion syndrome 6 (hepatocerebral type), MIM#256810",
"entity_name": "MPV17",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:57:42.025466+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.659",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MPV17 were set to ",
"entity_name": "MPV17",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:57:22.398067+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPL as ready",
"entity_name": "MPL",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:57:22.386895+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpl has been classified as Green List (High Evidence).",
"entity_name": "MPL",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:57:20.101803+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.658",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MPL were changed from Thrombocytopenia, congenital amegakaryocytic, 604498 (3) to Amegakaryocytic thrombocytopenia, congenital, 1, MIM# 604498",
"entity_name": "MPL",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:57:10.502234+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.657",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MPL were set to ",
"entity_name": "MPL",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:56:51.479887+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPI as ready",
"entity_name": "MPI",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:56:51.473421+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpi has been classified as Green List (High Evidence).",
"entity_name": "MPI",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:56:49.134728+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.656",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MPI were changed from Congenital disorder of glycosylation, type Ib, 602579 (3) to Congenital disorder of glycosylation, type Ib, MIM# 602579",
"entity_name": "MPI",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:56:39.943918+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.655",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MPI were set to ",
"entity_name": "MPI",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:56:20.793155+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.654",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MOCS2 as ready",
"entity_name": "MOCS2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:56:20.783493+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.654",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mocs2 has been classified as Green List (High Evidence).",
"entity_name": "MOCS2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:56:18.649648+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.654",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MOCS2 were changed from Molybdenum cofactor deficiency B, 252160 (3) to Molybdenum cofactor deficiency B (MIM#252160)",
"entity_name": "MOCS2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:56:09.771194+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.653",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MOCS2 were set to ",
"entity_name": "MOCS2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:55:50.905721+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.652",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MOCS1 as ready",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:55:50.895937+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.652",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mocs1 has been classified as Green List (High Evidence).",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:55:49.055173+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.652",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MOCS1 were changed from Molybdenum cofactor deficiency A, 252150 (3) to Molybdenum cofactor deficiency A (MIM#252150)",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:55:39.455098+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.651",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MOCS1 were set to ",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:55:21.120242+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.650",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MMADHC as ready",
"entity_name": "MMADHC",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:55:21.110631+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.650",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mmadhc has been classified as Green List (High Evidence).",
"entity_name": "MMADHC",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:55:18.982276+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.650",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MMADHC were changed from Methylmalonic aciduria and homocystinuria, cblD type, 277410 (3) to Homocystinuria, cblD type, variant 1 MIM#277410; Methylmalonic aciduria and homocystinuria, cblD type MIM#277410; Methylmalonic aciduria, cblD type, variant 2 MIM#277410; Disorders of cobalamin absorption, transport and metabolism",
"entity_name": "MMADHC",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:55:03.168773+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.649",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MMADHC were set to ",
"entity_name": "MMADHC",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:54:43.250911+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.648",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MMACHC as ready",
"entity_name": "MMACHC",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:54:43.244000+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.648",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mmachc has been classified as Green List (High Evidence).",
"entity_name": "MMACHC",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:54:41.326905+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.648",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MMACHC were changed from Methylmalonic aciduria and homocystinuria, cblC type, 277400 (3) to Methylmalonic aciduria and homocystinuria, cblC type MIM#277400",
"entity_name": "MMACHC",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:54:32.611387+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.647",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MMACHC were set to ",
"entity_name": "MMACHC",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:54:12.512558+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.646",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MMAB as ready",
"entity_name": "MMAB",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:54:12.501899+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.646",
"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": "2025-05-09T13:54:09.993025+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.646",
"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": "2025-05-09T13:53:59.221907+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.645",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MMAB were set to ",
"entity_name": "MMAB",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:53:40.593881+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.644",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MMAA as ready",
"entity_name": "MMAA",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:53:40.587052+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.644",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mmaa has been classified as Green List (High Evidence).",
"entity_name": "MMAA",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:53:38.319641+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.644",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MMAA were changed from Methylmalonic aciduria, vitamin B12-responsive, 251100 (3) to Methylmalonic aciduria, vitamin B12-responsive, MIM#251100",
"entity_name": "MMAA",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:53:15.239419+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.643",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MLYCD as ready",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:53:15.231868+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.643",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mlycd has been classified as Green List (High Evidence).",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:53:12.467838+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.643",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MLYCD were changed from Malonyl-CoA decarboxylase deficiency, 248360 (3) to Malonyl-CoA decarboxylase deficiency, MIM#248360",
"entity_name": "MLYCD",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:52:49.345385+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.642",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MLC1 as ready",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:52:49.333078+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.642",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mlc1 has been classified as Green List (High Evidence).",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:52:45.554997+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.642",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MLC1 were changed from Megalencephalic leukoencephalopathy with subcortical cysts, 604004 (3) to Megalencephalic leukoencephalopathy with subcortical cysts 1, MIM #604004",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:52:36.476528+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.641",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MLC1 were set to ",
"entity_name": "MLC1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:52:16.531899+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.640",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MKS1 as ready",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:52:16.522421+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.640",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mks1 has been classified as Green List (High Evidence).",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:52:14.060100+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.640",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MKS1 were changed from Meckel syndrome 1, 249000 (3) to Bardet-Biedl syndrome 13 MIM#615990; Joubert syndrome 28 MIM#617121; Meckel syndrome 1 MIM#249000; Ciliopathy MONDO:0005308",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:52:04.151870+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.639",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MKS1 were set to ",
"entity_name": "MKS1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:51:43.438547+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.638",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MKKS as ready",
"entity_name": "MKKS",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:51:43.428135+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.638",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mkks has been classified as Green List (High Evidence).",
"entity_name": "MKKS",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:51:41.118395+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.638",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MKKS were changed from McKusick-Kaufman syndrome, 236700 (3) to Bardet-Biedl syndrome 6 MIM#605231; McKusick-Kaufman syndrome MIM#236700; MKKS-related ciliopathy MONDO:1040050",
"entity_name": "MKKS",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:51:31.389067+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.637",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MKKS were set to ",
"entity_name": "MKKS",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:51:10.828111+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.636",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MID1 as ready",
"entity_name": "MID1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:51:10.818331+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.636",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mid1 has been classified as Green List (High Evidence).",
"entity_name": "MID1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:51:08.013413+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.636",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MID1 were changed from Opitz GBBB syndrome, type I, 300000 (3) to Opitz GBBB syndrome MIM#300000; MONDO:0017138",
"entity_name": "MID1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:50:58.233131+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.635",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MID1 were set to ",
"entity_name": "MID1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:50:38.736597+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.634",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MFSD8 as ready",
"entity_name": "MFSD8",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:50:38.726259+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.634",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mfsd8 has been classified as Green List (High Evidence).",
"entity_name": "MFSD8",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:50:36.882639+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.634",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MFSD8 were changed from Ceroid lipofuscinosis, neuronal, 7, 610951 (3) to Ceroid lipofuscinosis, neuronal, 7, MIM# 610951; MONDO:0012588",
"entity_name": "MFSD8",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:50:23.913632+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.633",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MFSD8 were set to ",
"entity_name": "MFSD8",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:50:03.893868+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.632",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MFN2 as ready",
"entity_name": "MFN2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:50:03.881859+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.632",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mfn2 has been classified as Green List (High Evidence).",
"entity_name": "MFN2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:50:01.806114+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.632",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MFN2 were changed from Charcot-Marie-Tooth disease, axonal, type 2A2B, 617087 (3), Autosomal recessive to Lipomatosis, multiple symmetric, with or without peripheral neuropathy, MIM# 151800",
"entity_name": "MFN2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:49:51.040782+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.631",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MFN2 were set to ",
"entity_name": "MFN2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:49:27.352455+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.630",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: METTL23 as ready",
"entity_name": "METTL23",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:49:27.343055+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.630",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mettl23 has been classified as Green List (High Evidence).",
"entity_name": "METTL23",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:49:25.235192+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.630",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: METTL23 were changed from Mental retardation, autosomal recessive 44, 615942 (3) to Intellectual developmental disorder, autosomal recessive 44, MIM #615942",
"entity_name": "METTL23",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:49:15.565339+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.629",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: METTL23 were set to ",
"entity_name": "METTL23",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:48:53.971207+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.628",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MESP2 as ready",
"entity_name": "MESP2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:48:53.961217+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.628",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mesp2 has been classified as Green List (High Evidence).",
"entity_name": "MESP2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:48:51.907251+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.628",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MESP2 were changed from Spondylocostal dysostosis 2, autosomal recessive, 608681 (3) to Spondylocostal dysostosis 2, MIM #608681",
"entity_name": "MESP2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:48:42.203082+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.627",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MESP2 were set to ",
"entity_name": "MESP2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:48:14.280191+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.626",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MED17 as ready",
"entity_name": "MED17",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:48:14.270280+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.626",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: med17 has been classified as Green List (High Evidence).",
"entity_name": "MED17",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:48:08.461498+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.626",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MED17 were changed from Microcephaly, postnatal progressive, with seizures and brain atrophy, 613668 (3) to Microcephaly, postnatal progressive, with seizures and brain atrophy, MIM#613668",
"entity_name": "MED17",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:47:56.459654+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.625",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MED17 were set to ",
"entity_name": "MED17",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:47:26.587792+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MED12 as ready",
"entity_name": "MED12",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:47:26.578030+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: med12 has been classified as Green List (High Evidence).",
"entity_name": "MED12",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:47:24.583520+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.624",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MED12 were changed from Lujan-Fryns syndrome, 309520 (3) to MED12-related intellectual disability syndrome, MONDO:0100000",
"entity_name": "MED12",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:47:15.441182+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.623",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MED12 were set to ",
"entity_name": "MED12",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:46:53.794592+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.622",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MECP2 as ready",
"entity_name": "MECP2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:46:53.784797+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.622",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mecp2 has been classified as Green List (High Evidence).",
"entity_name": "MECP2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:46:51.679182+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.622",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MECP2 were changed from Encephalopathy, neonatal severe, 300673 (3) to Encephalopathy, neonatal severe MIM#300673; Intellectual developmental disorder, X-linked syndromic 13 MIM#300055; Intellectual developmental disorder, X-linked syndromic, Lubs type MIM#300260",
"entity_name": "MECP2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:46:41.292356+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.621",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MECP2 were set to ",
"entity_name": "MECP2",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:46:18.999809+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.620",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MCPH1 as ready",
"entity_name": "MCPH1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:46:18.984835+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.620",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mcph1 has been classified as Green List (High Evidence).",
"entity_name": "MCPH1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:46:17.023998+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.620",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MCPH1 were changed from Microcephaly 1, primary, autosomal recessive, 251200 (3) to Microcephaly 1, primary, autosomal recessive, MIM#251200",
"entity_name": "MCPH1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:46:07.169322+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.619",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MCPH1 were set to ",
"entity_name": "MCPH1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:45:45.988893+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.618",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MCOLN1 as ready",
"entity_name": "MCOLN1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:45:45.980392+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.618",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mcoln1 has been classified as Green List (High Evidence).",
"entity_name": "MCOLN1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:45:43.868323+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.618",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MCOLN1 were changed from Mucolipidosis IV, 252650 (3) to Mucolipidosis IV MIM#252650",
"entity_name": "MCOLN1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:45:34.415721+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.617",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MCOLN1 were set to ",
"entity_name": "MCOLN1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:44:52.257217+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.616",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MASP1 as ready",
"entity_name": "MASP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:44:52.247824+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.616",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: masp1 has been classified as Green List (High Evidence).",
"entity_name": "MASP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:44:50.007074+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.616",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MASP1 were changed from 3MC syndrome 1, 257920 (3) to 3MC syndrome 1, MIM# 257920",
"entity_name": "MASP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:44:40.897862+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.615",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MASP1 were set to ",
"entity_name": "MASP1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:44:16.999288+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.614",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MANBA as ready",
"entity_name": "MANBA",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:44:16.992068+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.614",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: manba has been classified as Green List (High Evidence).",
"entity_name": "MANBA",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:44:10.590263+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.614",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MANBA were changed from Mannosidosis, beta, 248510 (3) to Mannosidosis, beta, MIM#248510",
"entity_name": "MANBA",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:43:47.254495+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MAN2B1 as ready",
"entity_name": "MAN2B1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:43:47.243055+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: man2b1 has been classified as Green List (High Evidence).",
"entity_name": "MAN2B1",
"entity_type": "gene"
},
{
"created": "2025-05-09T13:43:45.193054+10:00",
"panel_name": "Prepair 500+",
"panel_id": 4225,
"panel_version": "1.613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MAN2B1 were changed from Mannosidosis, alpha-, types I and II, 248500 (3) to Mannosidosis, alpha-, types I and II, MIM# 248500; MONDO:0009561",
"entity_name": "MAN2B1",
"entity_type": "gene"
},
{
"created": "2025-05-09T10:43:35.190839+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LSM1 were changed from Neurodevelopmental disorder, MONDO:0700092, LSM1-related to FICUS syndrome, MIM# 621193",
"entity_name": "LSM1",
"entity_type": "gene"
},
{
"created": "2025-05-09T10:43:06.923991+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "1.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LSM1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: FICUS syndrome, MIM# 621193; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LSM1",
"entity_type": "gene"
}
]
}