{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2079","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2077","results":[{"created":"2019-12-01T18:03:15.696127+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DSE was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DSE","entity_type":"gene"},{"created":"2019-12-01T18:03:08.425748+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DSE as Red List (low evidence)","entity_name":"DSE","entity_type":"gene"},{"created":"2019-12-01T18:03:08.418329+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dse has been classified as Red List (Low Evidence).","entity_name":"DSE","entity_type":"gene"},{"created":"2019-12-01T18:02:54.794367+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DSE: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ehlers-Danlos syndrome, musculocontractural type 2, MIM#615539; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DSE","entity_type":"gene"},{"created":"2019-12-01T17:31:39.165776+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DPYS as ready","entity_name":"DPYS","entity_type":"gene"},{"created":"2019-12-01T17:31:39.158441+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dpys has been classified as Green List (High Evidence).","entity_name":"DPYS","entity_type":"gene"},{"created":"2019-12-01T17:31:29.666919+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DPYS were changed from  to Dihydropyrimidinuria, MIM#222748","entity_name":"DPYS","entity_type":"gene"},{"created":"2019-12-01T17:31:12.757648+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DPYS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPYS","entity_type":"gene"},{"created":"2019-12-01T17:30:52.575565+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DPYS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Dihydropyrimidinuria, MIM#222748; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPYS","entity_type":"gene"},{"created":"2019-12-01T17:28:28.540976+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DPYS as ready","entity_name":"DPYS","entity_type":"gene"},{"created":"2019-12-01T17:28:28.533405+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dpys has been classified as Green List (High Evidence).","entity_name":"DPYS","entity_type":"gene"},{"created":"2019-12-01T17:28:20.583383+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DPYS were changed from  to Dihydropyrimidinuria, MIM#222748","entity_name":"DPYS","entity_type":"gene"},{"created":"2019-12-01T17:28:09.124949+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DPYS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPYS","entity_type":"gene"},{"created":"2019-12-01T17:27:50.579184+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DPYS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Dihydropyrimidinuria, MIM#222748; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPYS","entity_type":"gene"},{"created":"2019-12-01T17:25:19.723752+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: DPP10: Added comment: Link to autism based on CNV data.; Changed publications: 28670437","entity_name":"DPP10","entity_type":"gene"},{"created":"2019-12-01T17:24:19.500029+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DPP10 as ready","entity_name":"DPP10","entity_type":"gene"},{"created":"2019-12-01T17:24:19.492272+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dpp10 has been classified as Red List (Low Evidence).","entity_name":"DPP10","entity_type":"gene"},{"created":"2019-12-01T17:24:13.874029+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DPP10 were set to ","entity_name":"DPP10","entity_type":"gene"},{"created":"2019-12-01T17:23:58.055477+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DPP10 as Red List (low evidence)","entity_name":"DPP10","entity_type":"gene"},{"created":"2019-12-01T17:23:58.047775+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dpp10 has been classified as Red List (Low Evidence).","entity_name":"DPP10","entity_type":"gene"},{"created":"2019-12-01T17:23:22.261087+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DPP10: Rating: RED; Mode of pathogenicity: None; Publications: 28670437; Phenotypes: ; Mode of inheritance: None","entity_name":"DPP10","entity_type":"gene"},{"created":"2019-12-01T17:17:23.165712+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DPH1 as ready","entity_name":"DPH1","entity_type":"gene"},{"created":"2019-12-01T17:17:23.157944+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dph1 has been classified as Green List (High Evidence).","entity_name":"DPH1","entity_type":"gene"},{"created":"2019-12-01T17:17:16.505150+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DPH1 were changed from  to Developmental delay with short stature, dysmorphic facial features, and sparse hair, MIM#616901","entity_name":"DPH1","entity_type":"gene"},{"created":"2019-12-01T17:17:05.161619+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DPH1 were set to ","entity_name":"DPH1","entity_type":"gene"},{"created":"2019-12-01T17:16:56.121033+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DPH1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPH1","entity_type":"gene"},{"created":"2019-12-01T17:16:39.137357+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DPH1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25558065, 26220823; Phenotypes: Developmental delay with short stature, dysmorphic facial features, and sparse hair, MIM#616901; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DPH1","entity_type":"gene"},{"created":"2019-12-01T17:08:47.528920+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DOK7 as ready","entity_name":"DOK7","entity_type":"gene"},{"created":"2019-12-01T17:08:47.521722+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dok7 has been classified as Red List (Low Evidence).","entity_name":"DOK7","entity_type":"gene"},{"created":"2019-12-01T17:08:40.684456+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DOK7 were changed from  to Myasthenic syndrome, congenital, 10, MIM#254300","entity_name":"DOK7","entity_type":"gene"},{"created":"2019-12-01T17:08:26.213850+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DOK7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DOK7","entity_type":"gene"},{"created":"2019-12-01T17:08:18.845518+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DOK7 as Red List (low evidence)","entity_name":"DOK7","entity_type":"gene"},{"created":"2019-12-01T17:08:18.837352+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dok7 has been classified as Red List (Low Evidence).","entity_name":"DOK7","entity_type":"gene"},{"created":"2019-12-01T17:08:02.831691+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DOK7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Myasthenic syndrome, congenital, 10, MIM#254300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DOK7","entity_type":"gene"},{"created":"2019-12-01T17:02:55.802567+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DOCK6 as ready","entity_name":"DOCK6","entity_type":"gene"},{"created":"2019-12-01T17:02:55.795012+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dock6 has been classified as Green List (High Evidence).","entity_name":"DOCK6","entity_type":"gene"},{"created":"2019-12-01T17:02:50.838983+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DOCK6 were changed from  to Adams-Oliver syndrome 2, MIM#614219","entity_name":"DOCK6","entity_type":"gene"},{"created":"2019-12-01T17:02:33.258522+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DOCK6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DOCK6","entity_type":"gene"},{"created":"2019-12-01T17:02:18.568830+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DOCK6: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Adams-Oliver syndrome 2, MIM#614219; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DOCK6","entity_type":"gene"},{"created":"2019-12-01T17:00:41.003510+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DOCK4 as ready","entity_name":"DOCK4","entity_type":"gene"},{"created":"2019-12-01T17:00:40.996296+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dock4 has been classified as Red List (Low Evidence).","entity_name":"DOCK4","entity_type":"gene"},{"created":"2019-12-01T17:00:30.208401+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DOCK4 as Red List (low evidence)","entity_name":"DOCK4","entity_type":"gene"},{"created":"2019-12-01T17:00:30.201073+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dock4 has been classified as Red List (Low Evidence).","entity_name":"DOCK4","entity_type":"gene"},{"created":"2019-12-01T17:00:16.516429+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DOCK4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"DOCK4","entity_type":"gene"},{"created":"2019-12-01T16:55:15.411308+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNM1L as ready","entity_name":"DNM1L","entity_type":"gene"},{"created":"2019-12-01T16:55:15.403626+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnm1l has been classified as Green List (High Evidence).","entity_name":"DNM1L","entity_type":"gene"},{"created":"2019-12-01T16:55:03.740488+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNM1L were changed from  to Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1, MIM#614388","entity_name":"DNM1L","entity_type":"gene"},{"created":"2019-12-01T16:54:47.475274+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNM1L was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"DNM1L","entity_type":"gene"},{"created":"2019-12-01T16:54:28.332853+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNM1L: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1, MIM#614388; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"DNM1L","entity_type":"gene"},{"created":"2019-12-01T16:51:12.154338+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAJC6 as ready","entity_name":"DNAJC6","entity_type":"gene"},{"created":"2019-12-01T16:51:12.147126+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajc6 has been classified as Red List (Low Evidence).","entity_name":"DNAJC6","entity_type":"gene"},{"created":"2019-12-01T16:51:05.756857+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAJC6 were changed from  to Parkinson disease 19a, juvenile-onset, MIM#615528","entity_name":"DNAJC6","entity_type":"gene"},{"created":"2019-12-01T16:50:51.371278+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAJC6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAJC6","entity_type":"gene"},{"created":"2019-12-01T16:50:40.222757+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.104","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNAJC6 as Red List (low evidence)","entity_name":"DNAJC6","entity_type":"gene"},{"created":"2019-12-01T16:50:40.215175+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.104","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajc6 has been classified as Red List (Low Evidence).","entity_name":"DNAJC6","entity_type":"gene"},{"created":"2019-12-01T16:50:23.723864+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DNAJC6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Parkinson disease 19a, juvenile-onset, MIM#615528; Mode of inheritance: None","entity_name":"DNAJC6","entity_type":"gene"},{"created":"2019-12-01T11:18:25.320467+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAJC12 as ready","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:18:25.311730+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajc12 has been classified as Green List (High Evidence).","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:18:14.744656+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAJC12 were changed from  to Hyperphenylalaninemia, mild, non-BH4-deficient, MIM#617384","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:18:06.552733+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DNAJC12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:15:44.857745+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAJC12 as ready","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:15:44.850037+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajc12 has been classified as Green List (High Evidence).","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:15:40.191874+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNAJC12 as Green List (high evidence)","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:15:40.184397+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajc12 has been classified as Green List (High Evidence).","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:14:54.558522+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DNAJC12 was added\ngene: DNAJC12 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list\nMode of inheritance for gene: DNAJC12 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: DNAJC12 were set to Hyperphenylalaninemia, mild, non-BH4-deficient, MIM#617384\nReview for gene: DNAJC12 was set to GREEN\nAdded comment: Highly variable neurological phenotype, including ID, dystonia, parkinsonism. Treatable. \nSources: Expert list","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:12:49.285716+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAJC12 as ready","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:12:49.278103+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajc12 has been classified as Green List (High Evidence).","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:12:39.590310+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNAJC12 as Green List (high evidence)","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:12:39.581849+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnajc12 has been classified as Green List (High Evidence).","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:12:09.925266+11:00","panel_name":"Early onset Parkinson disease_MelbourneGenomics_VCGS","panel_id":26,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DNAJC12 was added\ngene: DNAJC12 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review\nMode of inheritance for gene: DNAJC12 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: DNAJC12 were set to Hyperphenylalaninemia, mild, non-BH4-deficient, MIM#617384\nReview for gene: DNAJC12 was set to GREEN\nAdded comment: Highly variable neurological phenotype, including ID, dystonia, parkinsonism. \nSources: Expert Review","entity_name":"DNAJC12","entity_type":"gene"},{"created":"2019-12-01T11:04:39.359528+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DMPK as ready","entity_name":"DMPK","entity_type":"gene"},{"created":"2019-12-01T11:04:39.350368+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dmpk has been classified as Green List (High Evidence).","entity_name":"DMPK","entity_type":"gene"},{"created":"2019-12-01T11:04:35.272938+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DMPK were changed from  to Myotonic dystrophy 1, MIM#160900","entity_name":"DMPK","entity_type":"gene"},{"created":"2019-12-01T11:04:25.249969+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DMPK was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DMPK","entity_type":"gene"},{"created":"2019-12-01T11:04:09.189163+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DMPK: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Myotonic dystrophy 1, MIM#160900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DMPK","entity_type":"gene"},{"created":"2019-12-01T11:01:27.666758+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DLK1 as ready","entity_name":"DLK1","entity_type":"gene"},{"created":"2019-12-01T11:01:27.659275+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlk1 has been classified as Red List (Low Evidence).","entity_name":"DLK1","entity_type":"gene"},{"created":"2019-12-01T11:01:20.177634+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DLK1 as Red List (low evidence)","entity_name":"DLK1","entity_type":"gene"},{"created":"2019-12-01T11:01:20.169600+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlk1 has been classified as Red List (Low Evidence).","entity_name":"DLK1","entity_type":"gene"},{"created":"2019-12-01T11:01:06.623887+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DLK1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"DLK1","entity_type":"gene"},{"created":"2019-12-01T10:55:54.932364+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DLGAP2 as ready","entity_name":"DLGAP2","entity_type":"gene"},{"created":"2019-12-01T10:55:54.925420+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlgap2 has been classified as Red List (Low Evidence).","entity_name":"DLGAP2","entity_type":"gene"},{"created":"2019-12-01T10:55:48.601602+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DLGAP2 as Red List (low evidence)","entity_name":"DLGAP2","entity_type":"gene"},{"created":"2019-12-01T10:55:48.594395+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlgap2 has been classified as Red List (Low Evidence).","entity_name":"DLGAP2","entity_type":"gene"},{"created":"2019-12-01T10:55:35.730852+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DLGAP2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"DLGAP2","entity_type":"gene"},{"created":"2019-12-01T10:49:50.850594+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DLG4 as ready","entity_name":"DLG4","entity_type":"gene"},{"created":"2019-12-01T10:49:50.843527+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg4 has been classified as Red List (Low Evidence).","entity_name":"DLG4","entity_type":"gene"},{"created":"2019-12-01T10:49:41.827069+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DLG4 as Red List (low evidence)","entity_name":"DLG4","entity_type":"gene"},{"created":"2019-12-01T10:49:41.819963+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg4 has been classified as Red List (Low Evidence).","entity_name":"DLG4","entity_type":"gene"},{"created":"2019-12-01T10:49:23.790372+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DLG4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"DLG4","entity_type":"gene"},{"created":"2019-12-01T10:48:56.451588+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DLG4 as ready","entity_name":"DLG4","entity_type":"gene"},{"created":"2019-12-01T10:48:56.444163+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg4 has been classified as Red List (Low Evidence).","entity_name":"DLG4","entity_type":"gene"},{"created":"2019-12-01T10:48:51.590679+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DLG4 as Red List (low evidence)","entity_name":"DLG4","entity_type":"gene"},{"created":"2019-12-01T10:48:51.583150+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg4 has been classified as Red List (Low Evidence).","entity_name":"DLG4","entity_type":"gene"},{"created":"2019-12-01T10:48:37.776845+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DLG4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"DLG4","entity_type":"gene"},{"created":"2019-12-01T10:42:22.032417+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DLAT as ready","entity_name":"DLAT","entity_type":"gene"},{"created":"2019-12-01T10:42:22.018348+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlat has been classified as Green List (High Evidence).","entity_name":"DLAT","entity_type":"gene"},{"created":"2019-12-01T10:42:15.809237+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DLAT were changed from  to Pyruvate dehydrogenase E2 deficiency, MIM#245348","entity_name":"DLAT","entity_type":"gene"},{"created":"2019-12-01T10:42:00.127590+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DLAT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DLAT","entity_type":"gene"},{"created":"2019-12-01T10:41:44.698972+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DLAT: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pyruvate dehydrogenase E2 deficiency, MIM#245348; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DLAT","entity_type":"gene"}]}