{"count":221284,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=231","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=229","results":[{"created":"2025-05-09T13:58:52.109333+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.663","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MTFMT were set to ","entity_name":"MTFMT","entity_type":"gene"},{"created":"2025-05-09T13:58:31.142445+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.662","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MRE11 as ready","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-05-09T13:58:31.132613+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.662","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mre11 has been classified as Green List (High Evidence).","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-05-09T13:58:27.252658+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.662","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MRE11 were changed from Ataxia-telangiectasia-like disorder, 604391 (3) to Ataxia-telangiectasia-like disorder, MIM#604391","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-05-09T13:58:15.630601+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.661","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MRE11 were set to ","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-05-09T13:57:55.885901+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.660","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MPV17 as ready","entity_name":"MPV17","entity_type":"gene"},{"created":"2025-05-09T13:57:55.876232+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.660","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mpv17 has been classified as Green List (High Evidence).","entity_name":"MPV17","entity_type":"gene"},{"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"}]}