{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=281","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=279","results":[{"created":"2025-03-24T16:58:50.323446+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1734","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: skiv2l has been classified as Green List (High Evidence).","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2025-03-24T16:58:47.623496+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1734","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SKIV2L were changed from Trichohepatoenteric syndrome 2, 614602 (3) to Trichohepatoenteric syndrome 2, MIM# 614602","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2025-03-24T16:58:37.371379+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1733","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SKIV2L were set to ","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2025-03-24T16:58:11.961953+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1732","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SIL1 as ready","entity_name":"SIL1","entity_type":"gene"},{"created":"2025-03-24T16:58:11.955038+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1732","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sil1 has been classified as Green List (High Evidence).","entity_name":"SIL1","entity_type":"gene"},{"created":"2025-03-24T16:58:09.142305+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1732","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SIL1 were changed from Marinesco-Sjogren syndrome, 248800 (3) to Marinesco-Sjogren syndrome MIM#248800","entity_name":"SIL1","entity_type":"gene"},{"created":"2025-03-24T16:57:58.239731+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1731","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SIL1 were set to ","entity_name":"SIL1","entity_type":"gene"},{"created":"2025-03-24T16:57:29.092434+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1730","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SERPINH1 as ready","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2025-03-24T16:57:29.085872+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1730","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: serpinh1 has been classified as Green List (High Evidence).","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2025-03-24T16:57:14.867148+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1730","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SERPINH1 were changed from Orofaciodigital syndrome VI, 277170 (3) to Osteogenesis imperfecta, type X, MIM# 613848; Osteogenesis imperfecta type 10, MONDO:0013459","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2025-03-24T16:57:02.489511+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1729","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SERPINH1 were set to ","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2025-03-24T16:56:30.431242+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1728","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SEPSECS as ready","entity_name":"SEPSECS","entity_type":"gene"},{"created":"2025-03-24T16:56:30.425230+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1728","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sepsecs has been classified as Green List (High Evidence).","entity_name":"SEPSECS","entity_type":"gene"},{"created":"2025-03-24T16:56:27.126253+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1728","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SEPSECS were changed from Pontocerebellar hypoplasia type 2D, 613811 (3) to Pontocerebellar hypoplasia type 2D, MIM# 613811","entity_name":"SEPSECS","entity_type":"gene"},{"created":"2025-03-24T16:56:15.386003+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1727","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SEPSECS were set to ","entity_name":"SEPSECS","entity_type":"gene"},{"created":"2025-03-24T16:55:50.922943+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1726","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SELENON as ready","entity_name":"SELENON","entity_type":"gene"},{"created":"2025-03-24T16:55:50.913837+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1726","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: selenon has been classified as Green List (High Evidence).","entity_name":"SELENON","entity_type":"gene"},{"created":"2025-03-24T16:55:47.986314+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1726","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SELENON were changed from Muscular dystrophy, rigid spine, 1, 602771 (3) to Congenital myopathy 3 with rigid spine, MIM# 602771","entity_name":"SELENON","entity_type":"gene"},{"created":"2025-03-24T16:55:36.507566+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1725","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SELENON were set to ","entity_name":"SELENON","entity_type":"gene"},{"created":"2025-03-24T16:54:52.325420+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1724","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SCNN1A as ready","entity_name":"SCNN1A","entity_type":"gene"},{"created":"2025-03-24T16:54:52.318804+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1724","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: scnn1a has been classified as Green List (High Evidence).","entity_name":"SCNN1A","entity_type":"gene"},{"created":"2025-03-24T16:54:49.497113+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1724","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SCNN1A were changed from Pseudohypoaldosteronism, type I, 264350 (3) to Pseudohypoaldosteronism, type IB1, autosomal recessive, MIM# 264350","entity_name":"SCNN1A","entity_type":"gene"},{"created":"2025-03-24T16:54:32.545488+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1723","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SCNN1A were set to ","entity_name":"SCNN1A","entity_type":"gene"},{"created":"2025-03-24T16:53:39.307843+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1722","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RSPH4A as ready","entity_name":"RSPH4A","entity_type":"gene"},{"created":"2025-03-24T16:53:39.301420+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1722","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rsph4a has been classified as Green List (High Evidence).","entity_name":"RSPH4A","entity_type":"gene"},{"created":"2025-03-24T16:53:05.091152+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1722","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RSPH4A were changed from Ciliary dyskinesia, primary, 11, 612649 (3) to Ciliary dyskinesia, primary, 11, MIM# 612649","entity_name":"RSPH4A","entity_type":"gene"},{"created":"2025-03-24T16:52:50.963777+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1721","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RSPH4A were set to ","entity_name":"RSPH4A","entity_type":"gene"},{"created":"2025-03-24T16:51:18.063328+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1720","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PSPH as ready","entity_name":"PSPH","entity_type":"gene"},{"created":"2025-03-24T16:51:18.056802+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1720","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: psph has been classified as Green List (High Evidence).","entity_name":"PSPH","entity_type":"gene"},{"created":"2025-03-24T16:51:12.936463+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1720","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PSPH were changed from Phosphoserine phosphatase deficiency, 614023 (3) to Phosphoserine phosphatase deficiency , MIM# 614023","entity_name":"PSPH","entity_type":"gene"},{"created":"2025-03-24T16:50:50.424093+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1719","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PSPH were set to ","entity_name":"PSPH","entity_type":"gene"},{"created":"2025-03-24T16:49:56.279152+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1718","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PPT1 as ready","entity_name":"PPT1","entity_type":"gene"},{"created":"2025-03-24T16:49:56.272430+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1718","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppt1 has been classified as Green List (High Evidence).","entity_name":"PPT1","entity_type":"gene"},{"created":"2025-03-24T16:49:35.811422+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1718","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PPT1 were changed from Ceroid lipofuscinosis, neuronal, 1, 256730 (3) to Ceroid lipofuscinosis, neuronal, 1, MIM# 256730","entity_name":"PPT1","entity_type":"gene"},{"created":"2025-03-24T16:49:20.079165+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1717","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PPT1 were set to ","entity_name":"PPT1","entity_type":"gene"},{"created":"2025-03-24T16:48:38.340035+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1716","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POMK as ready","entity_name":"POMK","entity_type":"gene"},{"created":"2025-03-24T16:48:38.333761+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1716","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pomk has been classified as Green List (High Evidence).","entity_name":"POMK","entity_type":"gene"},{"created":"2025-03-24T16:48:35.088275+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1716","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POMK were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12, 615249 (3) to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12, MIM#615249","entity_name":"POMK","entity_type":"gene"},{"created":"2025-03-24T16:48:23.070263+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1715","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POMK were set to ","entity_name":"POMK","entity_type":"gene"},{"created":"2025-03-24T16:47:44.673004+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1714","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POLR3A as ready","entity_name":"POLR3A","entity_type":"gene"},{"created":"2025-03-24T16:47:44.666604+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1714","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: polr3a has been classified as Green List (High Evidence).","entity_name":"POLR3A","entity_type":"gene"},{"created":"2025-03-24T16:47:41.437802+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1714","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POLR3A were changed from Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism, 607694 (3) to Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism, MIM# 607694; Wiedemann-Rautenstrauch syndrome, MIM# 264090","entity_name":"POLR3A","entity_type":"gene"},{"created":"2025-03-24T16:47:24.418253+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1713","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POLR3A were set to ","entity_name":"POLR3A","entity_type":"gene"},{"created":"2025-03-24T16:46:42.275567+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1712","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLOD1 as ready","entity_name":"PLOD1","entity_type":"gene"},{"created":"2025-03-24T16:46:42.265887+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1712","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plod1 has been classified as Green List (High Evidence).","entity_name":"PLOD1","entity_type":"gene"},{"created":"2025-03-24T16:46:38.117623+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1712","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PLOD1 were changed from Ehlers-Danlos syndrome, type VI, 225400 (3) to Ehlers-Danlos syndrome, kyphoscoliotic type, 1, MIM# 225400","entity_name":"PLOD1","entity_type":"gene"},{"created":"2025-03-24T16:46:15.946182+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1711","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PLOD1 were set to ","entity_name":"PLOD1","entity_type":"gene"},{"created":"2025-03-24T16:45:50.361078+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1710","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLEC as ready","entity_name":"PLEC","entity_type":"gene"},{"created":"2025-03-24T16:45:50.354475+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1710","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plec has been classified as Green List (High Evidence).","entity_name":"PLEC","entity_type":"gene"},{"created":"2025-03-24T16:45:47.282199+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1710","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PLEC were changed from Epidermolysis bullosa simplex with pyloric atresia, 612138 (3) to Epidermolysis bullosa simplex 5D, generalized intermediate, autosomal recessive, MIM# 616487; Epidermolysis bullosa simplex 5B, with muscular dystrophy, MIM# 226670; Epidermolysis bullosa simplex 5C, with pyloric atresia MIM# 612138; Muscular dystrophy, limb-girdle, autosomal recessive 17, MIM# 613723","entity_name":"PLEC","entity_type":"gene"},{"created":"2025-03-24T16:45:34.037499+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1709","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PLEC were set to ","entity_name":"PLEC","entity_type":"gene"},{"created":"2025-03-24T16:44:50.927508+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1708","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PFKM as ready","entity_name":"PFKM","entity_type":"gene"},{"created":"2025-03-24T16:44:50.918584+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1708","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pfkm has been classified as Green List (High Evidence).","entity_name":"PFKM","entity_type":"gene"},{"created":"2025-03-24T16:44:46.414129+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1708","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PFKM were changed from Glycogen storage disease VII, 232800 (3) to Glycogen storage disease VII MIM#232800","entity_name":"PFKM","entity_type":"gene"},{"created":"2025-03-24T16:44:36.196178+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1707","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PFKM were set to ","entity_name":"PFKM","entity_type":"gene"},{"created":"2025-03-24T16:43:55.906125+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1706","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX6 as ready","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-03-24T16:43:55.900349+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1706","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex6 has been classified as Green List (High Evidence).","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-03-24T16:43:52.029919+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1706","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX6 were changed from Peroxisome biogenesis disorder 4A (Zellweger), 614862 to Peroxisome biogenesis disorder 4A (Zellweger), MIM# 614862; Peroxisome biogenesis disorder-4B, MIM# 614863","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-03-24T16:43:41.985887+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1705","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX6 were set to ","entity_name":"PEX6","entity_type":"gene"},{"created":"2025-03-24T16:43:15.427488+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1704","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX13 as ready","entity_name":"PEX13","entity_type":"gene"},{"created":"2025-03-24T16:43:15.420869+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1704","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex13 has been classified as Green List (High Evidence).","entity_name":"PEX13","entity_type":"gene"},{"created":"2025-03-24T16:43:12.805650+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1704","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX13 were changed from Peroxisome biogenesis disorder 11A (Zellweger), 614883 to Peroxisome biogenesis disorder 11A (Zellweger), MIM#614883; Peroxisome biogenesis disorder 11B, MIM#614885","entity_name":"PEX13","entity_type":"gene"},{"created":"2025-03-24T16:42:43.352837+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1703","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX12 as ready","entity_name":"PEX12","entity_type":"gene"},{"created":"2025-03-24T16:42:43.346878+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1703","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex12 has been classified as Green List (High Evidence).","entity_name":"PEX12","entity_type":"gene"},{"created":"2025-03-24T16:42:39.896902+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1703","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX12 were changed from Peroxisome biogenesis disorder 3A (Zellweger), 614859 to Peroxisome biogenesis disorder 3A (Zellweger), MIM#614859; Peroxisome biogenesis disorder 3B, MIM#266510","entity_name":"PEX12","entity_type":"gene"},{"created":"2025-03-24T16:42:12.764682+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1702","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEPD as ready","entity_name":"PEPD","entity_type":"gene"},{"created":"2025-03-24T16:42:12.755939+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1702","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pepd has been classified as Green List (High Evidence).","entity_name":"PEPD","entity_type":"gene"},{"created":"2025-03-24T16:42:10.006762+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1702","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEPD were changed from Prolidase deficiency, 170100 (3) to Prolidase deficiency, MIM# 170100","entity_name":"PEPD","entity_type":"gene"},{"created":"2025-03-24T16:42:00.096137+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1701","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEPD were set to ","entity_name":"PEPD","entity_type":"gene"},{"created":"2025-03-24T16:41:20.150787+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1700","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: P3H1 as ready","entity_name":"P3H1","entity_type":"gene"},{"created":"2025-03-24T16:41:20.144455+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1700","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: p3h1 has been classified as Green List (High Evidence).","entity_name":"P3H1","entity_type":"gene"},{"created":"2025-03-24T16:41:15.260252+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1700","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: P3H1 were changed from Osteogenesis imperfecta, type VIII, 610915 (3) to Osteogenesis imperfecta, type VIII, MIM#610915","entity_name":"P3H1","entity_type":"gene"},{"created":"2025-03-24T16:41:04.489349+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1699","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: P3H1 were set to ","entity_name":"P3H1","entity_type":"gene"},{"created":"2025-03-24T16:40:41.780427+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OTC as ready","entity_name":"OTC","entity_type":"gene"},{"created":"2025-03-24T16:40:41.773354+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: otc has been classified as Green List (High Evidence).","entity_name":"OTC","entity_type":"gene"},{"created":"2025-03-24T16:40:39.211930+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1698","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OTC were changed from Ornithine transcarbamylase deficiency, 311250 (3) to Ornithine transcarbamylase deficiency, MIM# 311250","entity_name":"OTC","entity_type":"gene"},{"created":"2025-03-24T16:40:26.791997+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1697","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OTC were set to ","entity_name":"OTC","entity_type":"gene"},{"created":"2025-03-24T16:40:01.472395+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1696","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ORC6 as ready","entity_name":"ORC6","entity_type":"gene"},{"created":"2025-03-24T16:40:01.462075+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1696","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: orc6 has been classified as Green List (High Evidence).","entity_name":"ORC6","entity_type":"gene"},{"created":"2025-03-24T16:39:58.058567+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1696","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ORC6 were changed from Meier-Gorlin syndrome 3, 613803 (3) to Meier-Gorlin syndrome 3 MIM#613803","entity_name":"ORC6","entity_type":"gene"},{"created":"2025-03-24T16:39:44.716533+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1695","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ORC6 were set to ","entity_name":"ORC6","entity_type":"gene"},{"created":"2025-03-24T16:39:11.784220+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1694","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ORAI1 as ready","entity_name":"ORAI1","entity_type":"gene"},{"created":"2025-03-24T16:39:11.778063+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1694","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: orai1 has been classified as Green List (High Evidence).","entity_name":"ORAI1","entity_type":"gene"},{"created":"2025-03-24T16:38:56.885139+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1694","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ORAI1 were changed from Immunodeficiency 9, 612782 (3) to Immunodeficiency 9, MIM#612782; Myopathy, tubular aggregate, 2, MIM#615883","entity_name":"ORAI1","entity_type":"gene"},{"created":"2025-03-24T16:38:47.189943+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1693","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ORAI1 were set to ","entity_name":"ORAI1","entity_type":"gene"},{"created":"2025-03-24T16:38:18.846936+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1692","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OPHN1 as ready","entity_name":"OPHN1","entity_type":"gene"},{"created":"2025-03-24T16:38:18.840462+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1692","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ophn1 has been classified as Green List (High Evidence).","entity_name":"OPHN1","entity_type":"gene"},{"created":"2025-03-24T16:38:16.174512+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1692","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OPHN1 were changed from Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance, 300486 (3) to Intellectual developmental disorder, X-linked syndromic, Billuart type MIM#300486; X-linked intellectual disability-cerebellar hypoplasia syndrome MONDO:0010337","entity_name":"OPHN1","entity_type":"gene"},{"created":"2025-03-24T16:38:03.699486+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1691","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OPHN1 were set to ","entity_name":"OPHN1","entity_type":"gene"},{"created":"2025-03-24T16:37:12.122002+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1690","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OFD1 as ready","entity_name":"OFD1","entity_type":"gene"},{"created":"2025-03-24T16:37:12.112376+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1690","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ofd1 has been classified as Green List (High Evidence).","entity_name":"OFD1","entity_type":"gene"},{"created":"2025-03-24T16:37:06.583937+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1690","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OFD1 were changed from Joubert syndrome 10, 300804 (3) to Joubert syndrome 10 MIM#300804; Simpson-Golabi-Behmel syndrome, type 2 MIM#300209","entity_name":"OFD1","entity_type":"gene"},{"created":"2025-03-24T16:36:56.346665+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1689","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OFD1 were set to ","entity_name":"OFD1","entity_type":"gene"},{"created":"2025-03-24T16:36:11.744488+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NYX as ready","entity_name":"NYX","entity_type":"gene"},{"created":"2025-03-24T16:36:11.738328+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nyx has been classified as Green List (High Evidence).","entity_name":"NYX","entity_type":"gene"},{"created":"2025-03-24T16:36:07.497641+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1688","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NYX were changed from Night blindness, congenital stationary (complete), 1A, X-linked, MIM #310500 to Night blindness, congenital stationary (complete), 1A, X-linked MIM310500","entity_name":"NYX","entity_type":"gene"},{"created":"2025-03-24T16:35:54.216702+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1687","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NYX were set to ","entity_name":"NYX","entity_type":"gene"},{"created":"2025-03-24T16:34:42.292443+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1686","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NT5C2 as ready","entity_name":"NT5C2","entity_type":"gene"},{"created":"2025-03-24T16:34:42.285484+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1686","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nt5c2 has been classified as Green List (High Evidence).","entity_name":"NT5C2","entity_type":"gene"},{"created":"2025-03-24T16:34:37.150316+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1686","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NT5C2 were changed from Spastic paraplegia 45, 613162 (3) to Spastic paraplegia 45, autosomal recessive, MIM# 613162","entity_name":"NT5C2","entity_type":"gene"}]}