{"count":221415,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=527","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=525","results":[{"created":"2023-11-02T17:06:59.770212+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Schimke immunoosseous dysplasia, 242900 (3) for gene: SMARCAL1","entity_name":"SMARCAL1","entity_type":"gene"},{"created":"2023-11-02T17:06:58.401769+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Lysinuric protein intolerance, 222700 (3) for gene: SLC7A7","entity_name":"SLC7A7","entity_type":"gene"},{"created":"2023-11-02T17:06:57.389749+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Cerebral creatine deficiency syndrome 1, 300352 (3) for gene: SLC6A8","entity_name":"SLC6A8","entity_type":"gene"},{"created":"2023-11-02T17:06:56.018488+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hyperekplexia 3, 614618 (3) for gene: SLC6A5","entity_name":"SLC6A5","entity_type":"gene"},{"created":"2023-11-02T17:06:54.595635+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Brown-Vialetto-Van Laere syndrome 1, 211530 (3) for gene: SLC52A3","entity_name":"SLC52A3","entity_type":"gene"},{"created":"2023-11-02T17:06:53.373122+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Brown-Vialetto-Van Laere syndrome 2, 614707 (3) for gene: SLC52A2","entity_name":"SLC52A2","entity_type":"gene"},{"created":"2023-11-02T17:06:52.385332+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Folate malabsorption, hereditary, 229050 (3) for gene: SLC46A1","entity_name":"SLC46A1","entity_type":"gene"},{"created":"2023-11-02T17:06:50.986746+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Albinism, oculocutaneous, type IV, 606574 (3) for gene: SLC45A2","entity_name":"SLC45A2","entity_type":"gene"},{"created":"2023-11-02T17:06:49.581979+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Acrodermatitis enteropathica, 201100 (3) for gene: SLC39A4","entity_name":"SLC39A4","entity_type":"gene"},{"created":"2023-11-02T17:06:48.599122+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis, 609218 (3) for gene: SLC38A8","entity_name":"SLC38A8","entity_type":"gene"},{"created":"2023-11-02T17:06:47.190268+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Glycogen storage disease Ib, 232220 (3) for gene: SLC37A4","entity_name":"SLC37A4","entity_type":"gene"},{"created":"2023-11-02T17:06:45.869148+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Arthrogryposis, mental retardation, and seizures (MIM615553) for gene: SLC35A3\nPublications for gene SLC35A3 were updated from 24031089; 28777481; 28328131 to 28777481; 28328131; 24031089","entity_name":"SLC35A3","entity_type":"gene"},{"created":"2023-11-02T17:06:44.483893+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Diarrhea 1, secretory chloride, congenital, 214700 (3) for gene: SLC26A3","entity_name":"SLC26A3","entity_type":"gene"},{"created":"2023-11-02T17:06:43.518092+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Achondrogenesis Ib, 600972 (3) for gene: SLC26A2","entity_name":"SLC26A2","entity_type":"gene"},{"created":"2023-11-02T17:06:42.173102+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, 238970 (3) for gene: SLC25A15","entity_name":"SLC25A15","entity_type":"gene"},{"created":"2023-11-02T17:06:40.894279+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Citrullinemia, type II, neonatal-onset, 605814 (3) for gene: SLC25A13","entity_name":"SLC25A13","entity_type":"gene"},{"created":"2023-11-02T17:06:39.998033+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Combined D-2- and L-2-hydroxyglutaric aciduria, 615182 (3) for gene: SLC25A1","entity_name":"SLC25A1","entity_type":"gene"},{"created":"2023-11-02T17:06:38.707814+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Carnitine deficiency, systemic primary, 212140 (3) for gene: SLC22A5","entity_name":"SLC22A5","entity_type":"gene"},{"created":"2023-11-02T17:06:37.283016+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, 616657 (3) for gene: SLC1A4","entity_name":"SLC1A4","entity_type":"gene"},{"created":"2023-11-02T17:06:35.876231+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), 607483 (3) for gene: SLC19A3","entity_name":"SLC19A3","entity_type":"gene"},{"created":"2023-11-02T17:06:34.894234+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Thiamine-responsive megaloblastic anemia syndrome, 249270 (3) for gene: SLC19A2","entity_name":"SLC19A2","entity_type":"gene"},{"created":"2023-11-02T17:06:33.582642+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Sialic acid storage disorder, infantile, 269920 (3) for gene: SLC17A5","entity_name":"SLC17A5","entity_type":"gene"},{"created":"2023-11-02T17:06:32.290376+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Allan-Herndon-Dudley syndrome for gene: SLC16A2","entity_name":"SLC16A2","entity_type":"gene"},{"created":"2023-11-02T17:06:31.384497+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Agenesis of the corpus callosum with peripheral neuropathy, 218000 (3) for gene: SLC12A6","entity_name":"SLC12A6","entity_type":"gene"},{"created":"2023-11-02T17:06:30.095602+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Bartter syndrome, type 1, 601678 (3) for gene: SLC12A1","entity_name":"SLC12A1","entity_type":"gene"},{"created":"2023-11-02T17:06:28.783629+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Trichohepatoenteric syndrome 2, 614602 (3) for gene: SKIV2L","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2023-11-02T17:06:27.395294+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Charcot-Marie-Tooth disease, type 4C, 601596 (3) for gene: SH3TC2","entity_name":"SH3TC2","entity_type":"gene"},{"created":"2023-11-02T17:06:26.570248+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mucopolysaccharidisis type IIIA (Sanfilippo A), 252900 (3) for gene: SGSH","entity_name":"SGSH","entity_type":"gene"},{"created":"2023-11-02T17:06:25.288314+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Muscular dystrophy, limb-girdle, type 2C, 253700 (3) for gene: SGCG","entity_name":"SGCG","entity_type":"gene"},{"created":"2023-11-02T17:06:24.083109+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Muscular dystrophy, limb-girdle, type 2F, 601287 (3) for gene: SGCD","entity_name":"SGCD","entity_type":"gene"},{"created":"2023-11-02T17:06:22.808846+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Muscular dystrophy, limb-girdle, type 2E, 604286 (3) for gene: SGCB","entity_name":"SGCB","entity_type":"gene"},{"created":"2023-11-02T17:06:21.876190+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Muscular dystrophy, limb-girdle, type 2D, 608099 (3) for gene: SGCA","entity_name":"SGCA","entity_type":"gene"},{"created":"2023-11-02T17:06:20.614577+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Orofaciodigital syndrome VI, 277170 (3) for gene: SERPINH1","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2023-11-02T17:06:19.220071+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome, 614739 (3) for gene: SERAC1","entity_name":"SERAC1","entity_type":"gene"},{"created":"2023-11-02T17:06:18.291799+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Pontocerebellar hypoplasia type 2D, 613811 (3) for gene: SEPSECS","entity_name":"SEPSECS","entity_type":"gene"},{"created":"2023-11-02T17:06:17.071333+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Dyserythropoietic anemia, congenital, type II, 224100 (3) for gene: SEC23B","entity_name":"SEC23B","entity_type":"gene"},{"created":"2023-11-02T17:06:15.771883+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Bardet-Biedl syndrome 16, 615993 (3) for gene: SDCCAG8","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2023-11-02T17:06:14.409050+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1, 604377 (3) for gene: SCO2","entity_name":"SCO2","entity_type":"gene"},{"created":"2023-11-02T17:06:13.475001+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Lathosterolosis, 607330 (3) for gene: SC5D","entity_name":"SC5D","entity_type":"gene"},{"created":"2023-11-02T17:06:12.175985+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Aicardi-Goutieres syndrome 5, 612952 (3) for gene: SAMHD1","entity_name":"SAMHD1","entity_type":"gene"},{"created":"2023-11-02T17:06:10.874816+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Spastic ataxia, Charlevoix-Saguenay type, 270550 (3) for gene: SACS","entity_name":"SACS","entity_type":"gene"},{"created":"2023-11-02T17:06:09.889123+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Neuromuscular disease, congenital, with uniform type 1 fiber, MIM# 117000; Central core disease, MIM# 117000 for gene: RYR1","entity_name":"RYR1","entity_type":"gene"},{"created":"2023-11-02T17:06:08.602561+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Dyskeratosis congenita, autosomal recessive 5, 615190 (3) for gene: RTEL1","entity_name":"RTEL1","entity_type":"gene"},{"created":"2023-11-02T17:06:07.287754+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Coffin-Lowry syndrome for gene: RPS6KA3","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2023-11-02T17:06:05.886528+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Meckel syndrome 5, 611561 (3) for gene: RPGRIP1L","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2023-11-02T17:06:04.889207+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leber congenital amaurosis 2, 204100 (3) for gene: RPE65","entity_name":"RPE65","entity_type":"gene"},{"created":"2023-11-02T17:06:03.133392+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Retinitis pigmentosa 2, 312600 (3) for gene: RP2","entity_name":"RP2","entity_type":"gene"},{"created":"2023-11-02T17:06:01.202095+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Aicardi-Goutieres syndrome 3, 610329 (3) for gene: RNASEH2C","entity_name":"RNASEH2C","entity_type":"gene"},{"created":"2023-11-02T17:06:00.071452+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Aicardi-Goutieres syndrome 2, 610181 (3) for gene: RNASEH2B","entity_name":"RNASEH2B","entity_type":"gene"},{"created":"2023-11-02T17:05:58.672757+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Aicardi-Goutieres syndrome 4, 610333 (3) for gene: RNASEH2A","entity_name":"RNASEH2A","entity_type":"gene"},{"created":"2023-11-02T17:05:57.423288+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Cartilage-hair hypoplasia, 250250 (3) for gene: RMRP","entity_name":"RMRP","entity_type":"gene"},{"created":"2023-11-02T17:05:56.003263+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Combined oxidative phosphorylation deficiency 11, 614922 (3) for gene: RMND1","entity_name":"RMND1","entity_type":"gene"},{"created":"2023-11-02T17:05:54.892846+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leber congenital amaurosis 13, 612712 (3) for gene: RDH12","entity_name":"RDH12","entity_type":"gene"},{"created":"2023-11-02T17:05:53.674829+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Seckel syndrome 2, 606744 (3) for gene: RBBP8","entity_name":"RBBP8","entity_type":"gene"},{"created":"2023-11-02T17:05:52.389838+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Microphthalmia, isolated 3, 611038 (3) for gene: RAX","entity_name":"RAX","entity_type":"gene"},{"created":"2023-11-02T17:05:51.090370+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Pontocerebellar hypoplasia, type 6, 611523 (3) for gene: RARS2","entity_name":"RARS2","entity_type":"gene"},{"created":"2023-11-02T17:05:49.987596+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Fetal akinesia deformation sequence, 208150 (3) for gene: RAPSN","entity_name":"RAPSN","entity_type":"gene"},{"created":"2023-11-02T17:05:48.670609+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Severe combined immunodeficiency, B cell-negative, 601457 (3) for gene: RAG2\nPublications for gene RAG2 were updated from 26996199; 30046960 to 30046960; 26996199","entity_name":"RAG2","entity_type":"gene"},{"created":"2023-11-02T17:05:47.364390+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Severe combined immunodeficiency, B cell-negative, 601457 (3) for gene: RAG1","entity_name":"RAG1","entity_type":"gene"},{"created":"2023-11-02T17:05:46.373364+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Warburg micro syndrome 2, 614225 (3) for gene: RAB3GAP2","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2023-11-02T17:05:44.874070+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Warburg micro syndrome 1, 600118 (3) for gene: RAB3GAP1","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2023-11-02T17:05:43.568993+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Carpenter syndrome, 201000 (3) for gene: RAB23","entity_name":"RAB23","entity_type":"gene"},{"created":"2023-11-02T17:05:42.275209+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Warburg micro syndrome 3, 614222 (3) for gene: RAB18","entity_name":"RAB18","entity_type":"gene"},{"created":"2023-11-02T17:05:41.296424+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hyperphenylalaninemia, BH4-deficient, C, 261630 (3) for gene: QDPR","entity_name":"QDPR","entity_type":"gene"},{"created":"2023-11-02T17:05:40.063995+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mitochondrial myopathy and sideroblastic anemia 1, 600462 (3) for gene: PUS1","entity_name":"PUS1","entity_type":"gene"},{"created":"2023-11-02T17:05:38.603964+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hyperphenylalaninemia, BH4-deficient, A, 261640 (3) for gene: PTS","entity_name":"PTS","entity_type":"gene"},{"created":"2023-11-02T17:05:37.586548+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Metachromatic leukodystrophy due to SAP-b deficiency, 249900 (3) for gene: PSAP","entity_name":"PSAP","entity_type":"gene"},{"created":"2023-11-02T17:05:36.265533+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Arts syndrome, 301835 (3) for gene: PRPS1","entity_name":"PRPS1","entity_type":"gene"},{"created":"2023-11-02T17:05:34.887776+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Pituitary hormone deficiency, combined, 2, 262600 (3) for gene: PROP1","entity_name":"PROP1","entity_type":"gene"},{"created":"2023-11-02T17:05:33.667697+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hemophagocytic lymphohistiocytosis, familial, 2, 603553 (3) for gene: PRF1","entity_name":"PRF1","entity_type":"gene"},{"created":"2023-11-02T17:05:32.690342+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Brittle cornea syndrome 2, 614170 (3) for gene: PRDM5","entity_name":"PRDM5","entity_type":"gene"},{"created":"2023-11-02T17:05:31.374954+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Renpenning syndrome, 309500 (3) for gene: PQBP1","entity_name":"PQBP1","entity_type":"gene"},{"created":"2023-11-02T17:05:30.005606+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Ceroid lipofuscinosis, neuronal, 1, 256730 (3) for gene: PPT1","entity_name":"PPT1","entity_type":"gene"},{"created":"2023-11-02T17:05:29.096931+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Pituitary hormone deficiency, combined, 1, 613038 (3) for gene: POU1F1","entity_name":"POU1F1","entity_type":"gene"},{"created":"2023-11-02T17:05:27.781464+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, 201750 (3) for gene: POR","entity_name":"POR","entity_type":"gene"},{"created":"2023-11-02T17:05:26.507823+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2, 613150 (3) for gene: POMT2","entity_name":"POMT2","entity_type":"gene"},{"created":"2023-11-02T17:05:25.133639+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1, 236670 (3) for gene: POMT1","entity_name":"POMT1","entity_type":"gene"},{"created":"2023-11-02T17:05:24.097597+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3, 253280 (3) for gene: POMGNT1","entity_name":"POMGNT1","entity_type":"gene"},{"created":"2023-11-02T17:05:22.804738+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism, 614381 (3) for gene: POLR3B","entity_name":"POLR3B","entity_type":"gene"},{"created":"2023-11-02T17:05:21.497435+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Treacher Collins syndrome 3, 248390 (3) for gene: POLR1C","entity_name":"POLR1C","entity_type":"gene"},{"created":"2023-11-02T17:05:20.265978+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mitochondrial DNA depletion syndrome 4A (Alpers type), 203700 (3) for gene: POLG","entity_name":"POLG","entity_type":"gene"},{"created":"2023-11-02T17:05:19.288564+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Pyridoxamine 5'-phosphate oxidase deficiency, 610090 (3) for gene: PNPO","entity_name":"PNPO","entity_type":"gene"},{"created":"2023-11-02T17:05:17.781176+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Microcephaly, seizures, and developmental delay, 613402 (3) for gene: PNKP","entity_name":"PNKP","entity_type":"gene"},{"created":"2023-11-02T17:05:16.410039+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Congenital disorder of glycosylation, type Ia, 212065 (3) for gene: PMM2","entity_name":"PMM2","entity_type":"gene"},{"created":"2023-11-02T17:05:15.409457+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Epilepsy, early-onset, vitamin B6-dependent, 617290 (3), Autosomal recessive for gene: PLPBP","entity_name":"PLPBP","entity_type":"gene"},{"created":"2023-11-02T17:05:13.994012+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Pelizaeus-Merzbacher disease, 312080 (3) for gene: PLP1","entity_name":"PLP1","entity_type":"gene"},{"created":"2023-11-02T17:05:12.664481+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Ehlers-Danlos syndrome, type VI, 225400 (3) for gene: PLOD1","entity_name":"PLOD1","entity_type":"gene"},{"created":"2023-11-02T17:05:11.376816+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Neurodegeneration with brain iron accumulation 2B MIM#610217; Infantile neuroaxonal dystrophy 1 MIM#256600 for gene: PLA2G6","entity_name":"PLA2G6","entity_type":"gene"},{"created":"2023-11-02T17:05:10.402558+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Polycystic kidney and hepatic disease, 263200 (3) for gene: PKHD1","entity_name":"PKHD1","entity_type":"gene"},{"created":"2023-11-02T17:05:09.067941+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Multiple congenital anomalies-hypotonia-seizures syndrome 3 for gene: PIGT","entity_name":"PIGT","entity_type":"gene"},{"created":"2023-11-02T17:05:07.674516+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Multiple congenital anomalies-hypotonia-seizures syndrome 1, 614080 (3) for gene: PIGN","entity_name":"PIGN","entity_type":"gene"},{"created":"2023-11-02T17:05:06.611473+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mental retardation, autosomal recessive 53, 616917 (3) for gene: PIGG","entity_name":"PIGG","entity_type":"gene"},{"created":"2023-11-02T17:05:05.295690+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Joubert syndrome 33 (MIM#617767) for gene: PIBF1\nPublications for gene PIBF1 were updated from 26167768; 30858804; 29695797; 33004012 to 29695797; 33004012; 30858804; 26167768","entity_name":"PIBF1","entity_type":"gene"},{"created":"2023-11-02T17:05:03.995151+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Refsum disease, 266500 (3) for gene: PHYH","entity_name":"PHYH","entity_type":"gene"},{"created":"2023-11-02T17:05:02.699341+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Neu-Laxova syndrome1, 256520 (3) for gene: PHGDH","entity_name":"PHGDH","entity_type":"gene"},{"created":"2023-11-02T17:05:01.621103+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Mental retardation syndrome, X-linked, Siderius type, 300263 (3) for gene: PHF8","entity_name":"PHF8","entity_type":"gene"},{"created":"2023-11-02T17:05:00.129255+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Immunodeficiency 23, 615816 (3) for gene: PGM3","entity_name":"PGM3","entity_type":"gene"},{"created":"2023-11-02T17:04:58.793590+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Congenital disorder of glycosylation, type It, 614921 (3) for gene: PGM1","entity_name":"PGM1","entity_type":"gene"},{"created":"2023-11-02T17:04:57.818156+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Phosphoglycerate kinase 1 deficiency, 300653 (3) for gene: PGK1\nPublications for gene PGK1 were updated from 16567715; 30887539; 22348148; 28580215 to 22348148; 16567715; 28580215; 30887539","entity_name":"PGK1","entity_type":"gene"},{"created":"2023-11-02T17:04:56.572125+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.3","user_name":"Seb Lunke","item_type":"entity","text":"Added phenotypes Hyperphosphatasia with mental retardation syndrome 3, 614207 (3) for gene: PGAP2","entity_name":"PGAP2","entity_type":"gene"}]}