{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=309","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=307","results":[{"created":"2025-01-17T07:54:52.306822+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1064","user_name":"Michelle Torres","item_type":"entity","text":"reviewed gene: PDHA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22142326; Phenotypes: Pyruvate dehydrogenase E1-alpha deficiency MIM#312170; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"PDHA1","entity_type":"gene"},{"created":"2025-01-17T07:52:58.120178+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1064","user_name":"Michelle Torres","item_type":"entity","text":"Deleted their review","entity_name":"PDHA1","entity_type":"gene"},{"created":"2025-01-16T19:43:17.961186+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1064","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ELP1 as ready","entity_name":"ELP1","entity_type":"gene"},{"created":"2025-01-16T19:43:17.947446+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1064","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: elp1 has been classified as Green List (High Evidence).","entity_name":"ELP1","entity_type":"gene"},{"created":"2025-01-16T19:43:14.497418+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1064","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ELP1 were changed from Dysautonomia, familial, 223900 (3) to Dysautonomia, familial MIM#223900; Hereditary sensory and autonomic neuropathy type III (HSAN3)","entity_name":"ELP1","entity_type":"gene"},{"created":"2025-01-16T19:43:02.884747+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1063","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ELP1 were set to ","entity_name":"ELP1","entity_type":"gene"},{"created":"2025-01-16T19:42:37.542711+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1062","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EOGT as ready","entity_name":"EOGT","entity_type":"gene"},{"created":"2025-01-16T19:42:37.522989+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1062","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eogt has been classified as Green List (High Evidence).","entity_name":"EOGT","entity_type":"gene"},{"created":"2025-01-16T19:42:33.807956+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1062","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EOGT were changed from Adams-Oliver syndrome 4, 615297 (3) to Adams-Oliver syndrome 4, MIM#615297","entity_name":"EOGT","entity_type":"gene"},{"created":"2025-01-16T19:42:21.785801+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1061","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EOGT were set to ","entity_name":"EOGT","entity_type":"gene"},{"created":"2025-01-16T19:41:29.703388+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1060","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCE as ready","entity_name":"FANCE","entity_type":"gene"},{"created":"2025-01-16T19:41:29.689458+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1060","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fance has been classified as Green List (High Evidence).","entity_name":"FANCE","entity_type":"gene"},{"created":"2025-01-16T19:41:25.492991+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1060","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCE were changed from Fanconi anemia, complementation group E, 600901 (3) to Fanconi anaemia, complementation group E, MIM#600901","entity_name":"FANCE","entity_type":"gene"},{"created":"2025-01-16T19:41:09.697153+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1059","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCE were set to ","entity_name":"FANCE","entity_type":"gene"},{"created":"2025-01-16T19:39:17.356381+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1058","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXN1 as ready","entity_name":"FOXN1","entity_type":"gene"},{"created":"2025-01-16T19:39:17.336137+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1058","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxn1 has been classified as Green List (High Evidence).","entity_name":"FOXN1","entity_type":"gene"},{"created":"2025-01-16T19:39:12.440242+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1058","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FOXN1 were changed from T-cell immunodeficiency, congenital alopecia, and nail dystrophy, 601705 (3) to T-cell immunodeficiency, congenital alopecia, and nail dystrophy MIM#601705","entity_name":"FOXN1","entity_type":"gene"},{"created":"2025-01-16T19:38:58.295724+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1057","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXN1 were set to ","entity_name":"FOXN1","entity_type":"gene"},{"created":"2025-01-16T19:25:59.895885+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1056","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GJA1 as ready","entity_name":"GJA1","entity_type":"gene"},{"created":"2025-01-16T19:25:59.880026+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1056","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gja1 has been classified as Green List (High Evidence).","entity_name":"GJA1","entity_type":"gene"},{"created":"2025-01-16T19:25:54.620914+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1056","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GJA1 were changed from Hypoplastic left heart syndrome 1, 241550 (3) to Craniometaphyseal dysplasia, autosomal recessive MIM#218400; Oculodentodigital dysplasia, autosomal recessive MIM#257850","entity_name":"GJA1","entity_type":"gene"},{"created":"2025-01-16T19:25:42.374109+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1055","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GJA1 were set to ","entity_name":"GJA1","entity_type":"gene"},{"created":"2025-01-16T19:24:47.381012+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1054","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GLIS3 as ready","entity_name":"GLIS3","entity_type":"gene"},{"created":"2025-01-16T19:24:47.366845+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1054","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: glis3 has been classified as Green List (High Evidence).","entity_name":"GLIS3","entity_type":"gene"},{"created":"2025-01-16T19:24:43.963707+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1054","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GLIS3 were changed from Diabetes mellitus, neonatal, with congenital hypothyroidism, 610199 (3) to Diabetes mellitus, neonatal, with congenital hypothyroidism MIM#610199","entity_name":"GLIS3","entity_type":"gene"},{"created":"2025-01-16T19:24:30.309708+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1053","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GLIS3 were set to ","entity_name":"GLIS3","entity_type":"gene"},{"created":"2025-01-16T19:23:59.380289+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1052","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GPSM2 as ready","entity_name":"GPSM2","entity_type":"gene"},{"created":"2025-01-16T19:23:59.370908+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1052","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gpsm2 has been classified as Green List (High Evidence).","entity_name":"GPSM2","entity_type":"gene"},{"created":"2025-01-16T19:23:56.012243+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1052","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GPSM2 were changed from Chudley-McCullough syndrome, 604213 (3) to Chudley-McCullough syndrome, MIM#604213","entity_name":"GPSM2","entity_type":"gene"},{"created":"2025-01-16T19:23:35.880471+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1051","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GPSM2 were set to ","entity_name":"GPSM2","entity_type":"gene"},{"created":"2025-01-16T19:22:59.986785+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1050","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GRHPR were set to 28569194; 10484776; 10484776; 24116921","entity_name":"GRHPR","entity_type":"gene"},{"created":"2025-01-16T19:21:34.017427+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1049","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSPG2 as ready","entity_name":"HSPG2","entity_type":"gene"},{"created":"2025-01-16T19:21:34.000751+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1049","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hspg2 has been classified as Green List (High Evidence).","entity_name":"HSPG2","entity_type":"gene"},{"created":"2025-01-16T19:21:30.826383+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1049","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSPG2 were changed from Schwartz-Jampel syndrome, type 1, 255800 (3) to Schwartz-Jampel syndrome, type 1, MIM# 255800; Dyssegmental dysplasia, Silverman-Handmaker type, MIM# 224410","entity_name":"HSPG2","entity_type":"gene"},{"created":"2025-01-16T19:21:14.485657+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1048","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HSPG2 were set to ","entity_name":"HSPG2","entity_type":"gene"},{"created":"2025-01-16T19:20:42.496035+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1047","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TBX22 as ready","entity_name":"TBX22","entity_type":"gene"},{"created":"2025-01-16T19:20:42.482675+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1047","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tbx22 has been classified as Red List (Low Evidence).","entity_name":"TBX22","entity_type":"gene"},{"created":"2025-01-16T19:20:27.477273+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1047","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TBX22 were set to ","entity_name":"TBX22","entity_type":"gene"},{"created":"2025-01-16T19:20:10.737051+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1046","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TBX22: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TBX22","entity_type":"gene"},{"created":"2025-01-16T19:18:48.489859+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1046","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IGHMBP2 as ready","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2025-01-16T19:18:48.479148+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1046","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ighmbp2 has been classified as Green List (High Evidence).","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2025-01-16T19:18:35.492942+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1046","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IGHMBP2 were changed from Neuronopathy, distal hereditary motor, type VI, 604320 (3) to Neuronopathy, distal hereditary motor, autosomal recessive 1 MIM#604320; Charcot-Marie-Tooth disease, axonal, type 2S MIM#616155","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2025-01-16T19:18:20.520532+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1045","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IGHMBP2 were set to ","entity_name":"IGHMBP2","entity_type":"gene"},{"created":"2025-01-16T19:17:54.266088+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1044","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL10RB as ready","entity_name":"IL10RB","entity_type":"gene"},{"created":"2025-01-16T19:17:54.251988+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1044","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il10rb has been classified as Green List (High Evidence).","entity_name":"IL10RB","entity_type":"gene"},{"created":"2025-01-16T19:17:38.235211+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1044","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IL10RB were set to 22549091","entity_name":"IL10RB","entity_type":"gene"},{"created":"2025-01-16T19:17:09.976412+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1043","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBE2T as ready","entity_name":"UBE2T","entity_type":"gene"},{"created":"2025-01-16T19:17:09.961972+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1043","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ube2t has been classified as Green List (High Evidence).","entity_name":"UBE2T","entity_type":"gene"},{"created":"2025-01-16T19:17:06.731363+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1043","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBE2T were changed from Fanconi anemia, complementation group T, 616435 (3) to Fanconi anaemia, complementation group T, MIM#616435","entity_name":"UBE2T","entity_type":"gene"},{"created":"2025-01-16T19:16:50.917756+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1042","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBE2T were set to ","entity_name":"UBE2T","entity_type":"gene"},{"created":"2025-01-16T19:16:03.930372+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1041","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KATNB1 as ready","entity_name":"KATNB1","entity_type":"gene"},{"created":"2025-01-16T19:16:03.913673+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1041","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: katnb1 has been classified as Green List (High Evidence).","entity_name":"KATNB1","entity_type":"gene"},{"created":"2025-01-16T19:13:23.793442+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1041","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KATNB1 were changed from Lissencephaly 6, with microcephaly, 616212 (3) to Lissencephaly 6, with microcephaly, MIM#616212","entity_name":"KATNB1","entity_type":"gene"},{"created":"2025-01-16T19:13:12.696968+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1040","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KATNB1 were set to ","entity_name":"KATNB1","entity_type":"gene"},{"created":"2025-01-16T17:39:16.164288+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1039","user_name":"Michelle Torres","item_type":"entity","text":"reviewed gene: PDHA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22142326; Phenotypes: Pyruvate dehydrogenase E1-alpha deficiency MIM#312170; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDHA1","entity_type":"gene"},{"created":"2025-01-16T17:28:02.729922+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1039","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: JUP as ready","entity_name":"JUP","entity_type":"gene"},{"created":"2025-01-16T17:28:02.708760+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1039","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: jup has been classified as Green List (High Evidence).","entity_name":"JUP","entity_type":"gene"},{"created":"2025-01-16T17:27:59.624019+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1039","user_name":"Michelle Torres","item_type":"entity","text":"reviewed gene: ORC6: Rating: GREEN; Mode of pathogenicity: None; Publications: 21358632, 22333897, 25691413, 26139588; Phenotypes: Meier-Gorlin syndrome 3 MIM#613803; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ORC6","entity_type":"gene"},{"created":"2025-01-16T17:27:58.554817+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1039","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: JUP were changed from Naxos disease, 601214 (3) to Naxos disease MIM#601214","entity_name":"JUP","entity_type":"gene"},{"created":"2025-01-16T17:27:46.455889+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1038","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: JUP were set to ","entity_name":"JUP","entity_type":"gene"},{"created":"2025-01-16T17:26:35.284167+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1037","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LDHA as ready","entity_name":"LDHA","entity_type":"gene"},{"created":"2025-01-16T17:26:35.263846+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1037","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ldha has been classified as Green List (High Evidence).","entity_name":"LDHA","entity_type":"gene"},{"created":"2025-01-16T17:26:31.915033+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1037","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LDHA were changed from Glycogen storage disease XI, 612933 (3) to Glycogen storage disease XI MIM#612933","entity_name":"LDHA","entity_type":"gene"},{"created":"2025-01-16T17:26:19.650988+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1036","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LDHA were set to ","entity_name":"LDHA","entity_type":"gene"},{"created":"2025-01-16T17:25:43.319316+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1035","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMA2 as ready","entity_name":"LAMA2","entity_type":"gene"},{"created":"2025-01-16T17:25:43.298032+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1035","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lama2 has been classified as Green List (High Evidence).","entity_name":"LAMA2","entity_type":"gene"},{"created":"2025-01-16T17:25:36.669694+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1035","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LAMA2 were changed from Muscular dystrophy, congenital merosin-deficient, 607855 (3) to Muscular dystrophy, congenital, merosin deficient or partially deficient, MIM# 607855; Muscular dystrophy, limb-girdle, autosomal recessive 23, MIM# 618138","entity_name":"LAMA2","entity_type":"gene"},{"created":"2025-01-16T17:25:23.075964+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1034","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LAMA2 were set to ","entity_name":"LAMA2","entity_type":"gene"},{"created":"2025-01-16T17:24:56.175549+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1033","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYB5R3 as ready","entity_name":"CYB5R3","entity_type":"gene"},{"created":"2025-01-16T17:24:56.165437+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1033","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyb5r3 has been classified as Green List (High Evidence).","entity_name":"CYB5R3","entity_type":"gene"},{"created":"2025-01-16T17:24:52.925979+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1033","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CYB5R3 were changed from Methemoglobinemia, type I, 250800 (3) to Methemoglobinaemia, type II (MIM# 250800)","entity_name":"CYB5R3","entity_type":"gene"},{"created":"2025-01-16T17:24:37.085725+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1032","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CYB5R3 were set to ","entity_name":"CYB5R3","entity_type":"gene"},{"created":"2025-01-16T17:21:52.095208+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1031","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GALC as ready","entity_name":"GALC","entity_type":"gene"},{"created":"2025-01-16T17:21:52.085726+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1031","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: galc has been classified as Green List (High Evidence).","entity_name":"GALC","entity_type":"gene"},{"created":"2025-01-16T17:21:41.157194+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1031","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GALC were changed from Krabbe disease, 245200 (3) to Krabbe disease, MIM# 245200; MONDO:0009499","entity_name":"GALC","entity_type":"gene"},{"created":"2025-01-16T17:20:29.208415+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1030","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GALC were set to ","entity_name":"GALC","entity_type":"gene"},{"created":"2025-01-16T17:19:57.009136+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1029","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GORAB as ready","entity_name":"GORAB","entity_type":"gene"},{"created":"2025-01-16T17:19:56.993830+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1029","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gorab has been classified as Green List (High Evidence).","entity_name":"GORAB","entity_type":"gene"},{"created":"2025-01-16T17:19:48.510616+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1029","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GORAB were changed from Geroderma osteodysplasticum, 231070 (3) to Geroderma osteodysplasticum, MIM#231070; MONDO:0009271","entity_name":"GORAB","entity_type":"gene"},{"created":"2025-01-16T17:19:29.702190+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1028","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GORAB were set to ","entity_name":"GORAB","entity_type":"gene"},{"created":"2025-01-16T17:18:50.785800+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.46","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TAOK2 as ready","entity_name":"TAOK2","entity_type":"gene"},{"created":"2025-01-16T17:18:50.767299+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.46","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taok2 has been classified as Green List (High Evidence).","entity_name":"TAOK2","entity_type":"gene"},{"created":"2025-01-16T17:11:15.790826+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.46","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAOK2 as Green List (high evidence)","entity_name":"TAOK2","entity_type":"gene"},{"created":"2025-01-16T17:11:15.770379+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.46","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taok2 has been classified as Green List (High Evidence).","entity_name":"TAOK2","entity_type":"gene"},{"created":"2025-01-16T17:10:39.917915+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.45","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TAOK2 was added\ngene: TAOK2 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature\nMode of inheritance for gene: TAOK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: TAOK2 were set to 39737487\nPhenotypes for gene: TAOK2 were set to neurodevelopmental disorder, MONDO:0700092, TAOK2-related\nReview for gene: TAOK2 was set to GREEN\nAdded comment: PMID:39737487 reported 10 individuals with monoallelic TAOK2 variants and with a neurodevelopmental disorder. \nSources: Literature","entity_name":"TAOK2","entity_type":"gene"},{"created":"2025-01-16T17:09:16.633831+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2263","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TAOK2 were changed from Generalized verrucosis; abnormal T cell activation; autism to neurodevelopmental disorder, MONDO:0700092, TAOK2-related; Generalized verrucosis; abnormal T cell activation; autism","entity_name":"TAOK2","entity_type":"gene"},{"created":"2025-01-16T17:08:43.134022+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2262","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TAOK2 were set to 28385331; 29467497","entity_name":"TAOK2","entity_type":"gene"},{"created":"2025-01-16T17:08:04.402154+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2261","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TAOK2 as Green List (high evidence)","entity_name":"TAOK2","entity_type":"gene"},{"created":"2025-01-16T17:08:04.388967+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2261","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: taok2 has been classified as Green List (High Evidence).","entity_name":"TAOK2","entity_type":"gene"},{"created":"2025-01-16T17:03:00.712027+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1027","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PHGDH as ready","entity_name":"PHGDH","entity_type":"gene"},{"created":"2025-01-16T17:03:00.698877+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1027","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":"2025-01-16T16:56:21.462752+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1027","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":"2025-01-16T16:56:06.795698+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1026","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PHGDH were set to ","entity_name":"PHGDH","entity_type":"gene"},{"created":"2025-01-16T16:55:36.909486+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1025","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLOD2 as ready","entity_name":"PLOD2","entity_type":"gene"},{"created":"2025-01-16T16:55:36.893880+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1025","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plod2 has been classified as Green List (High Evidence).","entity_name":"PLOD2","entity_type":"gene"},{"created":"2025-01-16T16:54:14.357918+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1025","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PLOD2 were changed from Bruck syndrome 2, 609220 (3) to Bruck syndrome 2, MIM#609220","entity_name":"PLOD2","entity_type":"gene"},{"created":"2025-01-16T16:54:02.654650+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1024","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PLOD2 were set to ","entity_name":"PLOD2","entity_type":"gene"},{"created":"2025-01-16T16:53:33.086155+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1023","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SDCCAG8 as ready","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2025-01-16T16:53:33.068785+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1023","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sdccag8 has been classified as Green List (High Evidence).","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2025-01-16T16:53:27.653376+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1023","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SDCCAG8 were changed from Bardet-Biedl syndrome 16, 615993 (3) to Bardet-Biedl syndrome 16 (MIM# 615993); Senior-Loken syndrome 7 (MIM# 613615)","entity_name":"SDCCAG8","entity_type":"gene"}]}