{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2078","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2076","results":[{"created":"2019-12-02T06:23:50.104186+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ERF: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Chitayat syndrome, MIM#617180, Craniosynostosis 4, MIM#600775; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ERF","entity_type":"gene"},{"created":"2019-12-02T06:20:06.873681+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC4 as ready","entity_name":"ERCC4","entity_type":"gene"},{"created":"2019-12-02T06:20:06.866378+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc4 has been classified as Red List (Low Evidence).","entity_name":"ERCC4","entity_type":"gene"},{"created":"2019-12-02T06:20:02.646323+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC4 were changed from  to Xeroderma pigmentosum, group F, MIM#278760; XFE progeroid syndrome, MIM# 610965","entity_name":"ERCC4","entity_type":"gene"},{"created":"2019-12-02T06:19:43.034822+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ERCC4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ERCC4","entity_type":"gene"},{"created":"2019-12-02T06:19:31.345451+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ERCC4 as Red List (low evidence)","entity_name":"ERCC4","entity_type":"gene"},{"created":"2019-12-02T06:19:31.338076+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc4 has been classified as Red List (Low Evidence).","entity_name":"ERCC4","entity_type":"gene"},{"created":"2019-12-02T06:19:18.142628+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ERCC4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Xeroderma pigmentosum, group F, MIM#278760, XFE progeroid syndrome, MIM# 610965; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ERCC4","entity_type":"gene"},{"created":"2019-12-02T06:14:59.797621+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EPM2A as ready","entity_name":"EPM2A","entity_type":"gene"},{"created":"2019-12-02T06:14:59.789949+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: epm2a has been classified as Red List (Low Evidence).","entity_name":"EPM2A","entity_type":"gene"},{"created":"2019-12-02T06:14:55.822092+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EPM2A were changed from  to Epilepsy, progressive myoclonic 2A (Lafora), MIM#254780","entity_name":"EPM2A","entity_type":"gene"},{"created":"2019-12-02T06:14:31.371257+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EPM2A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EPM2A","entity_type":"gene"},{"created":"2019-12-02T06:14:18.182496+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EPM2A as Red List (low evidence)","entity_name":"EPM2A","entity_type":"gene"},{"created":"2019-12-02T06:14:18.171807+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: epm2a has been classified as Red List (Low Evidence).","entity_name":"EPM2A","entity_type":"gene"},{"created":"2019-12-02T06:14:01.390262+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.167","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: EPM2A: Changed rating: RED","entity_name":"EPM2A","entity_type":"gene"},{"created":"2019-12-02T06:13:46.684747+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.167","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EPM2A: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: Epilepsy, progressive myoclonic 2A (Lafora), MIM#254780; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"EPM2A","entity_type":"gene"},{"created":"2019-12-01T21:14:53.499451+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EOMES as ready","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:14:53.492395+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:14:49.862643+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EOMES were changed from  to Microcephaly","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:14:28.593867+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EOMES were set to ","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:14:06.227217+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EOMES was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:13:40.157407+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EOMES as Red List (low evidence)","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:13:40.148896+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:13:01.708316+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EOMES as ready","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:13:01.685394+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:12:52.322983+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EOMES were changed from  to Microcephaly","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:12:38.889331+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EOMES were set to ","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:12:24.097353+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EOMES was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:12:05.073288+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EOMES as Red List (low evidence)","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:12:05.064812+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:09:27.413598+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EOMES as ready","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:09:27.404098+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:09:22.521701+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EOMES were changed from  to Microcephaly","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:08:58.968816+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EOMES was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:08:40.643042+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EOMES as Red List (low evidence)","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:08:40.619372+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:08:23.042614+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EOMES as Red List (low evidence)","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:08:23.022905+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:08:05.071452+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EOMES as Red List (low evidence)","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:08:05.055425+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:07:47.695415+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EOMES was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:07:30.489689+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EOMES were set to ","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:07:13.367229+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EOMES as Red List (low evidence)","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:07:12.496335+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:06:45.364457+11:00","panel_name":"Polymicrogyria and schizencephaly_AustralianGenomics_VCGS","panel_id":18,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EOMES: Rating: RED; Mode of pathogenicity: None; Publications: 17353897; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:06:12.170518+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.167","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EOMES as ready","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:06:12.163296+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.167","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:05:52.488643+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.167","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EOMES were changed from  to Microcephaly","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:05:43.658220+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EOMES were set to ","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:05:33.115725+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EOMES was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:05:26.733204+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.164","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EOMES as Red List (low evidence)","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:05:26.725944+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.164","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T21:05:14.285487+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EOMES: Rating: RED; Mode of pathogenicity: None; Publications: 17353897; Phenotypes: Microcephaly; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"EOMES","entity_type":"gene"},{"created":"2019-12-01T20:57:58.755113+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EOGT as ready","entity_name":"EOGT","entity_type":"gene"},{"created":"2019-12-01T20:57:58.747254+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eogt has been classified as Red List (Low Evidence).","entity_name":"EOGT","entity_type":"gene"},{"created":"2019-12-01T20:57:53.909697+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EOGT were changed from  to Adams-Oliver syndrome 4, MIM#615297","entity_name":"EOGT","entity_type":"gene"},{"created":"2019-12-01T20:57:36.982335+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EOGT were set to ","entity_name":"EOGT","entity_type":"gene"},{"created":"2019-12-01T20:57:21.099335+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EOGT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EOGT","entity_type":"gene"},{"created":"2019-12-01T20:57:05.679273+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EOGT as Red List (low evidence)","entity_name":"EOGT","entity_type":"gene"},{"created":"2019-12-01T20:57:05.671225+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eogt has been classified as Red List (Low Evidence).","entity_name":"EOGT","entity_type":"gene"},{"created":"2019-12-01T20:56:53.206857+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EOGT: Rating: RED; Mode of pathogenicity: None; Publications: 31368252; Phenotypes: Adams-Oliver syndrome 4, MIM#615297; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"EOGT","entity_type":"gene"},{"created":"2019-12-01T20:53:01.849336+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2B5 were changed from  to Leukoencephalopathy with vanishing white matter, MIM#603896","entity_name":"EIF2B5","entity_type":"gene"},{"created":"2019-12-01T20:52:53.824733+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.158","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EIF2B5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EIF2B5","entity_type":"gene"},{"created":"2019-12-01T20:52:42.598310+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EIF2B5 as Red List (low evidence)","entity_name":"EIF2B5","entity_type":"gene"},{"created":"2019-12-01T20:52:42.590825+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b5 has been classified as Red List (Low Evidence).","entity_name":"EIF2B5","entity_type":"gene"},{"created":"2019-12-01T20:52:13.034252+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EIF2B5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukoencephalopathy with vanishing white matter, MIM#603896; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"EIF2B5","entity_type":"gene"},{"created":"2019-12-01T20:50:59.551899+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2B4 as ready","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2019-12-01T20:50:59.544673+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b4 has been classified as Red List (Low Evidence).","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2019-12-01T20:50:55.433005+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2B4 were changed from  to Leukoencephalopathy with vanishing white matter, MIM#603896","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2019-12-01T20:50:43.319321+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.155","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EIF2B4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2019-12-01T20:50:31.892235+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EIF2B4 as Red List (low evidence)","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2019-12-01T20:50:31.884915+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b4 has been classified as Red List (Low Evidence).","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2019-12-01T20:50:14.596729+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.153","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EIF2B4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukoencephalopathy with vanishing white matter, MIM#603896; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"EIF2B4","entity_type":"gene"},{"created":"2019-12-01T20:49:03.543907+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.153","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2B3 as ready","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2019-12-01T20:49:03.535866+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.153","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b3 has been classified as Red List (Low Evidence).","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2019-12-01T20:48:58.314397+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.153","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2B3 were changed from  to Leukoencephalopathy with vanishing white matter, MIM#603896","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2019-12-01T20:48:49.502489+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.152","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EIF2B3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2019-12-01T20:48:42.392080+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EIF2B3 as Red List (low evidence)","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2019-12-01T20:48:42.385010+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b3 has been classified as Red List (Low Evidence).","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2019-12-01T20:48:29.222062+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EIF2B3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukoencephalopathy with vanishing white matter, MIM#603896; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"EIF2B3","entity_type":"gene"},{"created":"2019-12-01T20:47:22.226021+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2B2 as ready","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2019-12-01T20:47:22.218227+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b2 has been classified as Red List (Low Evidence).","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2019-12-01T20:47:17.794606+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2B2 were changed from  to Leukoencephalopathy with vanishing white matter, MIM#603896","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2019-12-01T20:47:06.192895+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.149","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EIF2B2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2019-12-01T20:46:55.343167+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EIF2B2 as Red List (low evidence)","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2019-12-01T20:46:55.336194+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b2 has been classified as Red List (Low Evidence).","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2019-12-01T20:46:41.910072+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EIF2B2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukoencephalopathy with vanishing white matter, MIM#603896; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"EIF2B2","entity_type":"gene"},{"created":"2019-12-01T20:45:26.458536+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EIF2B1 as ready","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2019-12-01T20:45:26.450902+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b1 has been classified as Red List (Low Evidence).","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2019-12-01T20:45:21.824171+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EIF2B1 were changed from  to Leukoencephalopathy with vanishing white matter, MIM#603896","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2019-12-01T20:45:08.671225+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EIF2B1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2019-12-01T20:45:02.200326+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EIF2B1 as Red List (low evidence)","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2019-12-01T20:45:02.192674+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eif2b1 has been classified as Red List (Low Evidence).","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2019-12-01T20:44:50.183344+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: EIF2B1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukoencephalopathy with vanishing white matter, MIM#603896; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"EIF2B1","entity_type":"gene"},{"created":"2019-12-01T20:42:48.772343+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EFNB2 as ready","entity_name":"EFNB2","entity_type":"gene"},{"created":"2019-12-01T20:42:48.762871+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: efnb2 has been classified as Red List (Low Evidence).","entity_name":"EFNB2","entity_type":"gene"},{"created":"2019-12-01T20:42:43.514931+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EFNB2 were changed from  to Intellectual disability and congenital abnormalities","entity_name":"EFNB2","entity_type":"gene"},{"created":"2019-12-01T20:42:31.816806+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EFNB2 were set to ","entity_name":"EFNB2","entity_type":"gene"},{"created":"2019-12-01T20:42:20.627278+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EFNB2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"EFNB2","entity_type":"gene"},{"created":"2019-12-01T20:42:09.741621+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EFNB2 as Red List (low evidence)","entity_name":"EFNB2","entity_type":"gene"}]}