{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=293","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=291","results":[{"created":"2025-02-07T17:31:38.709188+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1561","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAPPC9 were set to ","entity_name":"TRAPPC9","entity_type":"gene"},{"created":"2025-02-07T17:30:58.728240+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1560","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UPF3B as ready","entity_name":"UPF3B","entity_type":"gene"},{"created":"2025-02-07T17:30:58.715141+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1560","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: upf3b has been classified as Green List (High Evidence).","entity_name":"UPF3B","entity_type":"gene"},{"created":"2025-02-07T17:30:54.427797+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1560","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UPF3B were changed from Mental retardation, X-linked, syndromic 14, 300676 (3) to Intellectual developmental disorder, X-linked syndromic 14 MIM#300676","entity_name":"UPF3B","entity_type":"gene"},{"created":"2025-02-07T17:30:33.517669+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1559","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UPF3B were set to ","entity_name":"UPF3B","entity_type":"gene"},{"created":"2025-02-07T17:30:05.274682+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1558","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WNK1 as ready","entity_name":"WNK1","entity_type":"gene"},{"created":"2025-02-07T17:30:05.258383+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1558","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wnk1 has been classified as Green List (High Evidence).","entity_name":"WNK1","entity_type":"gene"},{"created":"2025-02-07T17:30:02.323626+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1558","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WNK1 were changed from Neuropathy, hereditary sensory and autonomic, type II, 201300 (3) to Neuropathy, hereditary sensory and autonomic, type II MIM#201300","entity_name":"WNK1","entity_type":"gene"},{"created":"2025-02-07T17:29:46.330930+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1557","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WNK1 were set to ","entity_name":"WNK1","entity_type":"gene"},{"created":"2025-02-07T17:29:08.409982+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1556","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WNT7A as ready","entity_name":"WNT7A","entity_type":"gene"},{"created":"2025-02-07T17:29:08.399202+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1556","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wnt7a has been classified as Green List (High Evidence).","entity_name":"WNT7A","entity_type":"gene"},{"created":"2025-02-07T17:29:01.206128+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1556","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WNT7A were changed from Ulna and fibula, absence of, with severe limb deficiency, 276820 (3) to Fuhrmann syndrome MIM#228930; Ulna and fibula, absence of, with severe limb deficiency MIM#276820","entity_name":"WNT7A","entity_type":"gene"},{"created":"2025-02-07T17:28:34.125314+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1555","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WNT7A were set to ","entity_name":"WNT7A","entity_type":"gene"},{"created":"2025-02-07T17:28:06.965917+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1554","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZAP70 as ready","entity_name":"ZAP70","entity_type":"gene"},{"created":"2025-02-07T17:28:06.954960+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1554","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zap70 has been classified as Green List (High Evidence).","entity_name":"ZAP70","entity_type":"gene"},{"created":"2025-02-07T17:28:00.718403+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1554","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZAP70 were changed from Selective T-cell defect, 269840 (3) to Autoimmune disease, multisystem, infantile-onset, 2 MIM#617006; Immunodeficiency 48 MIM#269840","entity_name":"ZAP70","entity_type":"gene"},{"created":"2025-02-07T17:27:45.118346+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1553","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZAP70 were set to ","entity_name":"ZAP70","entity_type":"gene"},{"created":"2025-02-07T17:27:06.242393+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1552","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZC4H2 as ready","entity_name":"ZC4H2","entity_type":"gene"},{"created":"2025-02-07T17:27:06.218957+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1552","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zc4h2 has been classified as Green List (High Evidence).","entity_name":"ZC4H2","entity_type":"gene"},{"created":"2025-02-07T17:26:22.739411+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1552","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZC4H2 were changed from Wieacker-Wolff syndrome, 314580 (3) to Wieacker-Wolff syndrome MIM#314580","entity_name":"ZC4H2","entity_type":"gene"},{"created":"2025-02-07T17:26:10.165839+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1551","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZC4H2 were set to ","entity_name":"ZC4H2","entity_type":"gene"},{"created":"2025-02-07T17:25:58.440437+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1550","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ZC4H2 was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"ZC4H2","entity_type":"gene"},{"created":"2025-02-07T17:25:04.352886+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1549","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TK2 as ready","entity_name":"TK2","entity_type":"gene"},{"created":"2025-02-07T17:25:04.339073+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1549","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tk2 has been classified as Green List (High Evidence).","entity_name":"TK2","entity_type":"gene"},{"created":"2025-02-07T17:24:59.865496+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1549","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TK2 were changed from Mitochondrial DNA depletion syndrome 2 (myopathic type), 609560 (3) to Mitochondrial DNA depletion syndrome 2 (myopathic type) MIM#609560","entity_name":"TK2","entity_type":"gene"},{"created":"2025-02-07T17:24:46.204112+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1548","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TK2 were set to ","entity_name":"TK2","entity_type":"gene"},{"created":"2025-02-07T17:24:00.986307+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1547","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL17RA as ready","entity_name":"IL17RA","entity_type":"gene"},{"created":"2025-02-07T17:24:00.973093+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1547","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il17ra has been classified as Green List (High Evidence).","entity_name":"IL17RA","entity_type":"gene"},{"created":"2025-02-07T17:23:57.125345+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1547","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL17RA were changed from Immunodeficiency 51, 613953 (3), Autosomal recessive to Immunodeficiency 51, MIM #613953","entity_name":"IL17RA","entity_type":"gene"},{"created":"2025-02-07T17:23:42.598714+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1546","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IL17RA were set to ","entity_name":"IL17RA","entity_type":"gene"},{"created":"2025-02-07T17:23:11.029624+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1545","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ISCA2 as ready","entity_name":"ISCA2","entity_type":"gene"},{"created":"2025-02-07T17:23:11.013774+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1545","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: isca2 has been classified as Green List (High Evidence).","entity_name":"ISCA2","entity_type":"gene"},{"created":"2025-02-07T17:23:06.372454+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1545","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ISCA2 were changed from Multiple mitochondrial dysfunctions syndrome 4, 616370 (3) to Multiple mitochondrial dysfunctions syndrome 4, MIM #616370","entity_name":"ISCA2","entity_type":"gene"},{"created":"2025-02-07T17:22:51.895264+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1544","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ISCA2 were set to ","entity_name":"ISCA2","entity_type":"gene"},{"created":"2025-02-07T17:22:25.976078+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1543","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SBDS as ready","entity_name":"SBDS","entity_type":"gene"},{"created":"2025-02-07T17:22:25.940304+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1543","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sbds has been classified as Green List (High Evidence).","entity_name":"SBDS","entity_type":"gene"},{"created":"2025-02-07T17:21:56.287228+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1543","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SBDS were changed from Shwachman-Diamond syndrome, 260400 (3) to Shwachman-Diamond syndrome, MIM#260400","entity_name":"SBDS","entity_type":"gene"},{"created":"2025-02-07T17:21:44.589700+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1542","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SBDS were set to ","entity_name":"SBDS","entity_type":"gene"},{"created":"2025-02-07T17:21:17.243347+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1541","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIEZO2 as ready","entity_name":"PIEZO2","entity_type":"gene"},{"created":"2025-02-07T17:21:17.232208+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1541","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: piezo2 has been classified as Green List (High Evidence).","entity_name":"PIEZO2","entity_type":"gene"},{"created":"2025-02-07T17:21:11.813912+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1541","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PIEZO2 were changed from Arthrogryposis, distal, with impaired proprioception and touch, 617146 (3), Autosomal recessive to Arthrogryposis, distal, with impaired proprioception and touch, MIM#617146","entity_name":"PIEZO2","entity_type":"gene"},{"created":"2025-02-07T17:20:56.157811+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1540","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PIEZO2 were set to ","entity_name":"PIEZO2","entity_type":"gene"},{"created":"2025-02-07T17:20:25.842841+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1539","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PHF8 as ready","entity_name":"PHF8","entity_type":"gene"},{"created":"2025-02-07T17:20:25.830352+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1539","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: phf8 has been classified as Green List (High Evidence).","entity_name":"PHF8","entity_type":"gene"},{"created":"2025-02-07T17:20:21.851425+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1539","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PHF8 were changed from Mental retardation syndrome, X-linked, Siderius type, 300263 (3) to Intellectual developmental disorder, X-linked syndromic, Siderius type, MIM#300263","entity_name":"PHF8","entity_type":"gene"},{"created":"2025-02-07T17:19:58.364612+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1538","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PHF8 were set to ","entity_name":"PHF8","entity_type":"gene"},{"created":"2025-02-07T17:19:33.609759+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1537","user_name":"Zornitza Stark","item_type":"entity","text":"Tag for review tag was added to gene: ITGA3.","entity_name":"ITGA3","entity_type":"gene"},{"created":"2025-02-07T17:19:08.412344+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1537","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL1RAPL1 as ready","entity_name":"IL1RAPL1","entity_type":"gene"},{"created":"2025-02-07T17:19:08.387572+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1537","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il1rapl1 has been classified as Green List (High Evidence).","entity_name":"IL1RAPL1","entity_type":"gene"},{"created":"2025-02-07T17:19:05.156357+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1537","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL1RAPL1 were changed from Mental retardation, X-linked 21/34, 300143 (3) to Intellectual developmental disorder, X-linked 21, MIM#300143","entity_name":"IL1RAPL1","entity_type":"gene"},{"created":"2025-02-07T17:18:49.938241+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1536","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IL1RAPL1 were set to ","entity_name":"IL1RAPL1","entity_type":"gene"},{"created":"2025-02-07T17:18:26.833842+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1535","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF1C as ready","entity_name":"KIF1C","entity_type":"gene"},{"created":"2025-02-07T17:18:26.815841+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1535","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif1c has been classified as Green List (High Evidence).","entity_name":"KIF1C","entity_type":"gene"},{"created":"2025-02-07T17:18:23.407424+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1535","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF1C were changed from Spastic ataxia 2, autosomal recessive, 611302 (3) to Spastic ataxia 2, autosomal recessive, MIM#611302","entity_name":"KIF1C","entity_type":"gene"},{"created":"2025-02-07T17:17:59.027518+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1534","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF1C were set to ","entity_name":"KIF1C","entity_type":"gene"},{"created":"2025-02-07T17:17:32.425877+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1533","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SGCB as ready","entity_name":"SGCB","entity_type":"gene"},{"created":"2025-02-07T17:17:32.408567+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1533","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgcb has been classified as Green List (High Evidence).","entity_name":"SGCB","entity_type":"gene"},{"created":"2025-02-07T17:17:27.789913+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1533","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SGCB were changed from Muscular dystrophy, limb-girdle, type 2E, 604286 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 4 MIM#604286","entity_name":"SGCB","entity_type":"gene"},{"created":"2025-02-07T17:16:48.254619+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.63","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HECTD1 as ready","entity_name":"HECTD1","entity_type":"gene"},{"created":"2025-02-07T17:16:48.238863+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hectd1 has been classified as Green List (High Evidence).","entity_name":"HECTD1","entity_type":"gene"},{"created":"2025-02-07T17:16:30.292916+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.108","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HECTD1 as ready","entity_name":"HECTD1","entity_type":"gene"},{"created":"2025-02-07T17:16:30.280587+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.108","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hectd1 has been classified as Green List (High Evidence).","entity_name":"HECTD1","entity_type":"gene"},{"created":"2025-02-07T17:16:05.231259+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2298","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HECTD1 as ready","entity_name":"HECTD1","entity_type":"gene"},{"created":"2025-02-07T17:16:05.217816+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2298","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hectd1 has been classified as Green List (High Evidence).","entity_name":"HECTD1","entity_type":"gene"},{"created":"2025-02-07T17:15:30.052169+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1532","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POU1F1 as ready","entity_name":"POU1F1","entity_type":"gene"},{"created":"2025-02-07T17:15:30.030160+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1532","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pou1f1 has been classified as Green List (High Evidence).","entity_name":"POU1F1","entity_type":"gene"},{"created":"2025-02-07T17:15:26.737492+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1532","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POU1F1 were changed from Pituitary hormone deficiency, combined, 1, 613038 (3) to Pituitary hormone deficiency, combined or isolated, 1, MIM#613038","entity_name":"POU1F1","entity_type":"gene"},{"created":"2025-02-07T17:14:49.597088+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1531","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POU1F1 were set to ","entity_name":"POU1F1","entity_type":"gene"},{"created":"2025-02-07T17:14:24.734488+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1530","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TELO2 as ready","entity_name":"TELO2","entity_type":"gene"},{"created":"2025-02-07T17:14:24.712635+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1530","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: telo2 has been classified as Green List (High Evidence).","entity_name":"TELO2","entity_type":"gene"},{"created":"2025-02-07T17:14:20.974081+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1530","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TELO2 were changed from You-Hoover-Fong syndrome, 616954 (3), Autosomal recessive to You-Hoover-Fong syndrome, MIM#616954","entity_name":"TELO2","entity_type":"gene"},{"created":"2025-02-07T17:14:05.435225+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1529","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TELO2 were set to ","entity_name":"TELO2","entity_type":"gene"},{"created":"2025-02-07T17:13:31.949122+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.63","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARHGEF40 as ready","entity_name":"ARHGEF40","entity_type":"gene"},{"created":"2025-02-07T17:13:31.934784+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arhgef40 has been classified as Amber List (Moderate Evidence).","entity_name":"ARHGEF40","entity_type":"gene"},{"created":"2025-02-07T17:13:21.499551+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.63","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ARHGEF40 as Amber List (moderate evidence)","entity_name":"ARHGEF40","entity_type":"gene"},{"created":"2025-02-07T17:13:21.469493+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arhgef40 has been classified as Amber List (Moderate Evidence).","entity_name":"ARHGEF40","entity_type":"gene"},{"created":"2025-02-07T17:12:40.958597+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.62","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ARHGEF40: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ARHGEF40","entity_type":"gene"},{"created":"2025-02-07T17:11:58.450632+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2298","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARHGEF40 as ready","entity_name":"ARHGEF40","entity_type":"gene"},{"created":"2025-02-07T17:11:58.441184+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2298","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arhgef40 has been classified as Amber List (Moderate Evidence).","entity_name":"ARHGEF40","entity_type":"gene"},{"created":"2025-02-07T17:11:46.514105+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2298","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ARHGEF40 as Amber List (moderate evidence)","entity_name":"ARHGEF40","entity_type":"gene"},{"created":"2025-02-07T17:11:46.496153+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2298","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arhgef40 has been classified as Amber List (Moderate Evidence).","entity_name":"ARHGEF40","entity_type":"gene"},{"created":"2025-02-07T17:11:18.485755+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2297","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ARHGEF40: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ARHGEF40","entity_type":"gene"},{"created":"2025-02-07T17:10:27.549805+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1528","user_name":"Cassandra Muller","item_type":"entity","text":"reviewed gene: SLC4A4: Rating: GREEN; Mode of pathogenicity: None; Publications: 10545938, 15085340, 15471865; Phenotypes: Proximal renal tubular acidosis-ocular anomaly syndrome, 604278 (3); Mode of inheritance: None","entity_name":"SLC4A4","entity_type":"gene"},{"created":"2025-02-07T17:09:56.151275+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.62","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C12orf66 as ready","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:09:56.143797+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.62","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: New HGNC approved gene name is KICS2","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:09:56.093622+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.62","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c12orf66 has been classified as Green List (High Evidence).","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:09:34.679071+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.62","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: C12orf66.","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:09:07.227003+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2297","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C12orf66 as ready","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:09:07.218378+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2297","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: HGNC approved name: KICS2","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:09:07.116190+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2297","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c12orf66 has been classified as Green List (High Evidence).","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:08:40.891349+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2297","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: C12orf66.","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:08:07.559029+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.108","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C12orf66 as ready","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:08:07.546009+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.108","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: HGNC approved name is KICS2","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:08:07.471768+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.108","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c12orf66 has been classified as Green List (High Evidence).","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:07:54.661816+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.108","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: C12orf66.","entity_name":"C12orf66","entity_type":"gene"},{"created":"2025-02-07T17:07:15.932888+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1528","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMCO1 as ready","entity_name":"TMCO1","entity_type":"gene"},{"created":"2025-02-07T17:07:15.921674+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1528","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmco1 has been classified as Green List (High Evidence).","entity_name":"TMCO1","entity_type":"gene"},{"created":"2025-02-07T17:07:11.876183+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1528","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMCO1 were changed from Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome, 213980 (3) to Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1, MIM#213980","entity_name":"TMCO1","entity_type":"gene"},{"created":"2025-02-07T17:06:55.796195+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1527","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMCO1 were set to ","entity_name":"TMCO1","entity_type":"gene"},{"created":"2025-02-07T17:06:29.358104+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1526","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TULP1 as ready","entity_name":"TULP1","entity_type":"gene"}]}