{"count":221413,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=345","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=343","results":[{"created":"2024-11-15T15:23:52.365827+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6824","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: INPP5K as ready","entity_name":"INPP5K","entity_type":"gene"},{"created":"2024-11-15T15:23:52.355996+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6824","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: inpp5k has been classified as Green List (High Evidence).","entity_name":"INPP5K","entity_type":"gene"},{"created":"2024-11-15T15:23:47.539697+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6824","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: INPP5K were changed from  to congenital muscular dystrophy with cataracts and intellectual disability MONDO:0024607","entity_name":"INPP5K","entity_type":"gene"},{"created":"2024-11-15T15:23:02.902594+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6823","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: INPP5K were set to ","entity_name":"INPP5K","entity_type":"gene"},{"created":"2024-11-15T15:22:24.100594+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6822","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: INPP5K was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"INPP5K","entity_type":"gene"},{"created":"2024-11-15T15:21:30.318330+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6821","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IKBKG as ready","entity_name":"IKBKG","entity_type":"gene"},{"created":"2024-11-15T15:21:30.308298+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6821","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ikbkg has been classified as Green List (High Evidence).","entity_name":"IKBKG","entity_type":"gene"},{"created":"2024-11-15T15:21:17.745326+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6821","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IKBKG were changed from  to Incontinentia pigmenti MONDO:0010631","entity_name":"IKBKG","entity_type":"gene"},{"created":"2024-11-15T15:20:34.708010+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6820","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IKBKG were set to ","entity_name":"IKBKG","entity_type":"gene"},{"created":"2024-11-15T15:19:53.664988+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6819","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IKBKG was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"IKBKG","entity_type":"gene"},{"created":"2024-11-15T14:24:51.749924+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.547","user_name":"Cassandra Muller","item_type":"entity","text":"reviewed gene: EYS: Rating: RED; Mode of pathogenicity: None; Publications: 20537394, 31074760; Phenotypes: Retinitis pigmentosa 25 (MIM#602772); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"EYS","entity_type":"gene"},{"created":"2024-11-15T12:36:29.312327+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.547","user_name":"Lauren Rogers","item_type":"entity","text":"reviewed gene: ACE: Rating: GREEN; Mode of pathogenicity: None; Publications: 16116425, 22095942; Phenotypes: Renal tubular dysgenesis, MIM# 267430; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ACE","entity_type":"gene"},{"created":"2024-11-15T12:02:45.990695+11:00","panel_name":"Muscular dystrophy and myopathy_Paediatric","panel_id":141,"panel_version":"1.79","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RFC4 as ready","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T12:02:45.976366+11:00","panel_name":"Muscular dystrophy and myopathy_Paediatric","panel_id":141,"panel_version":"1.79","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rfc4 has been classified as Green List (High Evidence).","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T12:02:38.297324+11:00","panel_name":"Muscular dystrophy and myopathy_Paediatric","panel_id":141,"panel_version":"1.79","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RFC4 were changed from Morimoto-Ryu-Malicdan neuromuscular syndrome, MIM# 621010 to Morimoto-Ryu-Malicdan neuromuscular syndrome, MIM# 621010","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T12:02:09.642558+11:00","panel_name":"Muscular dystrophy and myopathy_Paediatric","panel_id":141,"panel_version":"1.79","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RFC4 were changed from RFC4-related multisystem disorder to Morimoto-Ryu-Malicdan neuromuscular syndrome, MIM# 621010","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T12:01:13.464130+11:00","panel_name":"Muscular dystrophy and myopathy_Paediatric","panel_id":141,"panel_version":"1.78","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RFC4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Morimoto-Ryu-Malicdan neuromuscular syndrome, MIM# 621010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T12:00:03.711889+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2145","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RFC4 as ready","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T12:00:03.674857+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2145","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rfc4 has been classified as Green List (High Evidence).","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T11:59:56.195443+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2145","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RFC4 were changed from RFC4-related multisystem disorder to Morimoto-Ryu-Malicdan neuromuscular syndrome, MIM# 621010","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T11:59:09.971031+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"1.73","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RFC4 as ready","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T11:59:09.953719+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"1.73","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rfc4 has been classified as Green List (High Evidence).","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T11:58:17.684109+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"1.73","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RFC4 were changed from RFC4-related multisystem disorder to Morimoto-Ryu-Malicdan neuromuscular syndrome, MIM# 621010","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T11:57:15.404284+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"1.72","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RFC4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Morimoto-Ryu-Malicdan neuromuscular syndrome, MIM# 621010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"RFC4","entity_type":"gene"},{"created":"2024-11-15T11:29:17.012159+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.294","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHRSX were changed from congenital disorder of glycosylation, MONDO:0015286, DHRSX-related to Congenital disorder of glycosylation, type 1DD, MIM# 301133","entity_name":"DHRSX","entity_type":"gene"},{"created":"2024-11-15T11:29:01.280856+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.293","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: DHRSX: Changed phenotypes: Congenital disorder of glycosylation, type 1DD, MIM# 301133","entity_name":"DHRSX","entity_type":"gene"},{"created":"2024-11-15T11:28:30.059419+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6818","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHRSX were changed from congenital disorder of glycosylation, MONDO:0015286, DHRSX-related to Congenital disorder of glycosylation, type 1DD, MIM# 301133","entity_name":"DHRSX","entity_type":"gene"},{"created":"2024-11-15T11:27:49.826820+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6817","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: DHRSX: Changed phenotypes: Congenital disorder of glycosylation, type 1DD, MIM# 301133","entity_name":"DHRSX","entity_type":"gene"},{"created":"2024-11-15T11:27:25.362616+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.206","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHRSX were changed from congenital disorder of glycosylation, MONDO:0015286, DHRSX-related to Congenital disorder of glycosylation, type 1DD, MIM# 301133","entity_name":"DHRSX","entity_type":"gene"},{"created":"2024-11-15T11:26:40.032582+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.205","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: DHRSX: Changed phenotypes: Congenital disorder of glycosylation, type 1DD, MIM# 301133","entity_name":"DHRSX","entity_type":"gene"},{"created":"2024-11-15T11:25:54.411828+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.73","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHRSX were changed from congenital disorder of glycosylation, MONDO:0015286, DHRSX-related to Congenital disorder of glycosylation, type 1DD, MIM# 301133","entity_name":"DHRSX","entity_type":"gene"},{"created":"2024-11-15T11:24:53.302093+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.72","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: DHRSX: Changed phenotypes: Congenital disorder of glycosylation, type 1DD, MIM# 301133","entity_name":"DHRSX","entity_type":"gene"},{"created":"2024-11-15T11:24:35.434737+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2144","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHRSX were changed from congenital disorder of glycosylation, MONDO:0015286 to Congenital disorder of glycosylation, type 1DD, MIM# 301133","entity_name":"DHRSX","entity_type":"gene"},{"created":"2024-11-15T11:23:34.968621+11:00","panel_name":"Congenital Disorders of Glycosylation","panel_id":68,"panel_version":"1.56","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHRSX were changed from congenital disorder of glycosylation, MONDO:0015286, DHRSX-related to Congenital disorder of glycosylation, type 1DD, MIM#\t301133","entity_name":"DHRSX","entity_type":"gene"},{"created":"2024-11-14T20:36:40.680269+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6817","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFT172 as ready","entity_name":"IFT172","entity_type":"gene"},{"created":"2024-11-14T20:36:40.670314+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6817","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ift172 has been classified as Green List (High Evidence).","entity_name":"IFT172","entity_type":"gene"},{"created":"2024-11-14T19:56:10.748252+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6817","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IFT172 were changed from  to Bardet-Biedl syndrome MONDO:0015229","entity_name":"IFT172","entity_type":"gene"},{"created":"2024-11-14T19:55:31.870735+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6816","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFT172 were set to ","entity_name":"IFT172","entity_type":"gene"},{"created":"2024-11-14T19:54:55.656809+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6815","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT172 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT172","entity_type":"gene"},{"created":"2024-11-14T19:53:58.327336+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6814","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IFIH1 as ready","entity_name":"IFIH1","entity_type":"gene"},{"created":"2024-11-14T19:53:58.309560+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6814","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ifih1 has been classified as Green List (High Evidence).","entity_name":"IFIH1","entity_type":"gene"},{"created":"2024-11-14T19:53:54.062539+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6814","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IFIH1 were changed from  to IFIH1-related type 1 interferonopathy MONDO:0700262","entity_name":"IFIH1","entity_type":"gene"},{"created":"2024-11-14T19:53:15.207462+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6813","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IFIH1 were set to ","entity_name":"IFIH1","entity_type":"gene"},{"created":"2024-11-14T19:50:50.013372+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6812","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFIH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"IFIH1","entity_type":"gene"},{"created":"2024-11-14T19:49:17.469520+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6811","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IDUA as ready","entity_name":"IDUA","entity_type":"gene"},{"created":"2024-11-14T19:49:17.456725+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6811","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: idua has been classified as Green List (High Evidence).","entity_name":"IDUA","entity_type":"gene"},{"created":"2024-11-14T19:48:48.221936+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6811","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IDUA were changed from  to mucopolysaccharidosis type 1 MONDO:0001586","entity_name":"IDUA","entity_type":"gene"},{"created":"2024-11-14T19:48:04.308506+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6810","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IDUA were set to 20301341","entity_name":"IDUA","entity_type":"gene"},{"created":"2024-11-14T19:47:29.343869+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6809","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IDUA were set to ","entity_name":"IDUA","entity_type":"gene"},{"created":"2024-11-14T19:39:45.814747+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6808","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IDUA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IDUA","entity_type":"gene"},{"created":"2024-11-14T19:38:42.949763+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6807","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IDS as ready","entity_name":"IDS","entity_type":"gene"},{"created":"2024-11-14T19:38:42.936858+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6807","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ids has been classified as Green List (High Evidence).","entity_name":"IDS","entity_type":"gene"},{"created":"2024-11-14T19:38:36.085434+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6807","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IDS were changed from  to mucopolysaccharidosis type 2 MONDO:0010674","entity_name":"IDS","entity_type":"gene"},{"created":"2024-11-14T19:36:07.314991+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6806","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IDS were set to ","entity_name":"IDS","entity_type":"gene"},{"created":"2024-11-14T18:59:46.222571+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6805","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IDS was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"IDS","entity_type":"gene"},{"created":"2024-11-14T18:58:57.424204+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6804","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IDH2 as ready","entity_name":"IDH2","entity_type":"gene"},{"created":"2024-11-14T18:58:57.393968+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6804","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: idh2 has been classified as Green List (High Evidence).","entity_name":"IDH2","entity_type":"gene"},{"created":"2024-11-14T18:58:47.209495+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6804","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IDH2 were changed from  to mitochondrial disease MONDO:0044970","entity_name":"IDH2","entity_type":"gene"},{"created":"2024-11-14T18:57:52.557841+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6803","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IDH2 were set to ","entity_name":"IDH2","entity_type":"gene"},{"created":"2024-11-14T18:57:06.916803+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6802","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IDH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"IDH2","entity_type":"gene"},{"created":"2024-11-14T18:56:18.206045+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6801","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HTRA2 as ready","entity_name":"HTRA2","entity_type":"gene"},{"created":"2024-11-14T18:56:18.194366+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6801","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: htra2 has been classified as Green List (High Evidence).","entity_name":"HTRA2","entity_type":"gene"},{"created":"2024-11-14T18:56:13.734549+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6801","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HTRA2 were changed from  to 3-methylglutaconic aciduria type 8 MONDO:0044723","entity_name":"HTRA2","entity_type":"gene"},{"created":"2024-11-14T18:55:27.850687+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6800","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HTRA2 were set to ","entity_name":"HTRA2","entity_type":"gene"},{"created":"2024-11-14T18:54:34.503890+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6799","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HTRA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HTRA2","entity_type":"gene"},{"created":"2024-11-14T18:53:29.436623+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6798","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSPD1 as ready","entity_name":"HSPD1","entity_type":"gene"},{"created":"2024-11-14T18:53:29.414883+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6798","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hspd1 has been classified as Green List (High Evidence).","entity_name":"HSPD1","entity_type":"gene"},{"created":"2024-11-14T18:52:33.125281+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6798","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSPD1 were changed from Leukodystrophy, hypomyelinating, 4, MIM# 612233 to Leukodystrophy, hypomyelinating, 4, MIM# 612233","entity_name":"HSPD1","entity_type":"gene"},{"created":"2024-11-14T18:30:22.518401+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6797","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSPD1 were changed from Leukodystrophy, hypomyelinating, 4, MIM# 612233 to Leukodystrophy, hypomyelinating, 4, MIM# 612233","entity_name":"HSPD1","entity_type":"gene"},{"created":"2024-11-14T18:29:44.190873+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6796","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSPD1 were changed from  to Leukodystrophy, hypomyelinating, 4, MIM# 612233","entity_name":"HSPD1","entity_type":"gene"},{"created":"2024-11-14T18:28:56.515912+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6795","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HSPD1 were set to ","entity_name":"HSPD1","entity_type":"gene"},{"created":"2024-11-14T18:28:15.086954+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6794","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HSPD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HSPD1","entity_type":"gene"},{"created":"2024-11-14T18:27:39.819528+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6793","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HSPD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 18571143, 27405012, 32532876, 28377887, 27405012, 11898127, 17420924; Phenotypes: Leukodystrophy, hypomyelinating, 4, MIM# 612233; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HSPD1","entity_type":"gene"},{"created":"2024-11-14T18:25:28.187710+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6793","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSD17B10 were changed from HSD10 mitochondrial disease MONDO:0010327 to HSD10 mitochondrial disease MONDO:0010327","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2024-11-14T18:25:12.768047+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6792","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSD17B10 as ready","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2024-11-14T18:25:12.753296+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6792","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hsd17b10 has been classified as Green List (High Evidence).","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2024-11-14T18:24:06.611160+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6792","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSD17B10 were changed from  to HSD10 mitochondrial disease MONDO:0010327","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2024-11-14T18:23:14.815722+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6791","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HSD17B10 were set to ","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2024-11-14T18:22:24.726232+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6790","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HSD17B10 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"HSD17B10","entity_type":"gene"},{"created":"2024-11-14T18:21:01.554461+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6789","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HPRT1 as ready","entity_name":"HPRT1","entity_type":"gene"},{"created":"2024-11-14T18:21:01.526598+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6789","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hprt1 has been classified as Green List (High Evidence).","entity_name":"HPRT1","entity_type":"gene"},{"created":"2024-11-14T18:20:56.742056+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6789","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HPRT1 were changed from  to Lesch-Nyhan syndrome MONDO:0010298","entity_name":"HPRT1","entity_type":"gene"},{"created":"2024-11-14T18:20:09.568781+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6788","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HPRT1 were set to ","entity_name":"HPRT1","entity_type":"gene"},{"created":"2024-11-14T18:19:26.961147+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6787","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HPRT1 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"HPRT1","entity_type":"gene"},{"created":"2024-11-14T18:18:30.494329+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6786","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HPD as ready","entity_name":"HPD","entity_type":"gene"},{"created":"2024-11-14T18:18:30.473665+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6786","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hpd has been classified as Green List (High Evidence).","entity_name":"HPD","entity_type":"gene"},{"created":"2024-11-14T18:18:22.582862+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6786","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HPD were changed from  to tyrosinemia type III MONDO:0010162","entity_name":"HPD","entity_type":"gene"},{"created":"2024-11-14T18:16:19.534730+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6785","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HPD were set to ","entity_name":"HPD","entity_type":"gene"},{"created":"2024-11-14T18:15:31.187987+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6784","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HPD was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HPD","entity_type":"gene"},{"created":"2024-11-14T18:14:42.776709+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6783","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HPD: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: tyrosinemia type III MONDO:0010162; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HPD","entity_type":"gene"},{"created":"2024-11-14T18:12:35.494007+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6783","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HOXA1 as ready","entity_name":"HOXA1","entity_type":"gene"},{"created":"2024-11-14T18:12:35.480282+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6783","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hoxa1 has been classified as Green List (High Evidence).","entity_name":"HOXA1","entity_type":"gene"},{"created":"2024-11-14T18:12:25.501199+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6783","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HOXA1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HOXA1","entity_type":"gene"},{"created":"2024-11-14T18:11:48.106732+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6782","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HOXA1 were set to ","entity_name":"HOXA1","entity_type":"gene"},{"created":"2024-11-14T18:11:10.202814+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6781","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HOXA1 were changed from  to Bosley-Salih-Alorainy syndrome, MIM#601536 and Athabaskan brainstem dysgenesis syndrome, MIM#601536","entity_name":"HOXA1","entity_type":"gene"},{"created":"2024-11-14T18:09:58.036956+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6780","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HNRNPK as ready","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2024-11-14T18:09:58.021999+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6780","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hnrnpk has been classified as Green List (High Evidence).","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2024-11-14T18:09:51.805981+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6780","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HNRNPK were changed from  to neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome (Au-Kline syndrome) MONDO:0018681","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2024-11-14T18:09:13.172607+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6779","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HNRNPK were set to ","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2024-11-14T18:07:52.511731+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6778","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HNRNPK was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HNRNPK","entity_type":"gene"}]}