{"count":220377,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2060","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2058","results":[{"created":"2019-12-08T07:58:53.100812+11:00","panel_name":"Combined immunodeficiency_MelbourneGenomics_VCGS","panel_id":223,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOP10 as ready","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:58:53.093928+11:00","panel_name":"Combined immunodeficiency_MelbourneGenomics_VCGS","panel_id":223,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nop10 has been classified as Red List (Low Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:58:48.892303+11:00","panel_name":"Combined immunodeficiency_MelbourneGenomics_VCGS","panel_id":223,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOP10 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:58:31.411298+11:00","panel_name":"Combined immunodeficiency_MelbourneGenomics_VCGS","panel_id":223,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOP10 were changed from  to Dyskeratosis congenita, autosomal recessive 1, MIM#224230","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:58:13.567350+11:00","panel_name":"Combined immunodeficiency_MelbourneGenomics_VCGS","panel_id":223,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:57:56.203224+11:00","panel_name":"Combined immunodeficiency_MelbourneGenomics_VCGS","panel_id":223,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOP10 were set to ","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:56:44.439676+11:00","panel_name":"Combined immunodeficiency_MelbourneGenomics_VCGS","panel_id":223,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NOP10 as Red List (low evidence)","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:56:44.431986+11:00","panel_name":"Combined immunodeficiency_MelbourneGenomics_VCGS","panel_id":223,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nop10 has been classified as Red List (Low Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:56:05.149724+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.202","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOP10 as ready","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:56:05.142362+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.202","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nop10 has been classified as Red List (Low Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:55:57.105707+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.202","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOP10 were changed from  to Dyskeratosis congenita, autosomal recessive 1, MIM#224230","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:55:42.182377+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.201","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOP10 were set to ","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:55:23.794457+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.200","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:55:04.419964+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.199","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NOP10 as Red List (low evidence)","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:55:04.411652+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.199","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nop10 has been classified as Red List (Low Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:54:38.361964+11:00","panel_name":"Cancer Predisposition_Paediatric_VCGS","panel_id":152,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOP10 as ready","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:54:38.353826+11:00","panel_name":"Cancer Predisposition_Paediatric_VCGS","panel_id":152,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nop10 has been classified as Red List (Low Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:54:28.111808+11:00","panel_name":"Cancer Predisposition_Paediatric_VCGS","panel_id":152,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:53:49.220451+11:00","panel_name":"Cancer Predisposition_Paediatric_VCGS","panel_id":152,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOP10 were changed from  to Dyskeratosis congenita, autosomal recessive 1, MIM#224230","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:53:11.233882+11:00","panel_name":"Cancer Predisposition_Paediatric_VCGS","panel_id":152,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOP10 were set to ","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:52:47.829503+11:00","panel_name":"Cancer Predisposition_Paediatric_VCGS","panel_id":152,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NOP10 as Red List (low evidence)","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:52:47.818142+11:00","panel_name":"Cancer Predisposition_Paediatric_VCGS","panel_id":152,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nop10 has been classified as Red List (Low Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:48:13.369509+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOP10 as ready","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:48:13.362149+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nop10 has been classified as Red List (Low Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:48:09.398125+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOP10 were changed from  to Dyskeratosis congenita, autosomal recessive 1, MIM#224230","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:47:49.463924+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOP10 were set to 17507419","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:47:21.293092+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOP10 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:47:00.423667+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NOP10 as Red List (low evidence)","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:47:00.414964+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nop10 has been classified as Red List (Low Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:46:43.990187+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOP10 were set to ","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:46:27.475313+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:46:11.175895+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NOP10 as Red List (low evidence)","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:46:11.131620+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nop10 has been classified as Red List (Low Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:45:41.957641+11:00","panel_name":"Bone Marrow Failure_VCGS","panel_id":56,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NOP10: Rating: RED; Mode of pathogenicity: None; Publications: 17507419; Phenotypes: Dyskeratosis congenita, autosomal recessive 1, MIM#224230; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:44:48.783237+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.874","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NOP10 as ready","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:44:48.775771+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.874","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nop10 has been classified as Red List (Low Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:44:43.467089+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.874","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NOP10 were changed from  to Dyskeratosis congenita, autosomal recessive 1, MIM#224230","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:44:29.799058+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.873","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NOP10 were set to ","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:44:20.250251+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.872","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:44:13.401622+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.871","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NOP10 as Red List (low evidence)","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:44:13.392706+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.871","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nop10 has been classified as Red List (Low Evidence).","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:44:00.124335+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.870","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NOP10: Rating: RED; Mode of pathogenicity: None; Publications: 17507419; Phenotypes: Dyskeratosis congenita, autosomal recessive 1, MIM#224230; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NOP10","entity_type":"gene"},{"created":"2019-12-08T07:39:45.583914+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NIN as ready","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:39:45.576987+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nin has been classified as Red List (Low Evidence).","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:39:38.074495+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NIN were changed from  to Seckel syndrome 7, MIM#614851","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:39:24.871275+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.196","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NIN were set to ","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:39:08.400195+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.195","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NIN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:38:45.584022+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.194","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NIN as Red List (low evidence)","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:38:45.575938+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.194","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nin has been classified as Red List (Low Evidence).","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:38:25.971456+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.193","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NIN: Rating: RED; Mode of pathogenicity: None; Publications: 22933543; Phenotypes: Seckel syndrome 7, MIM#614851; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:37:22.544644+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NIN as ready","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:37:22.537178+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nin has been classified as Red List (Low Evidence).","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:37:19.787387+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NIN were changed from  to Seckel syndrome 7, MIM#614851","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:37:00.059409+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NIN were set to ","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:36:38.513453+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NIN as Red List (low evidence)","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:36:38.506507+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nin has been classified as Red List (Low Evidence).","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:36:13.108325+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NIN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:35:56.930664+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NIN as Red List (low evidence)","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:35:56.868521+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nin has been classified as Red List (Low Evidence).","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:33:22.871714+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NIN as ready","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:33:22.862733+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nin has been classified as Red List (Low Evidence).","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:33:18.773641+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NIN were changed from  to Seckel syndrome 7, MIM#614851","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:32:57.684436+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NIN were set to ","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:32:34.169118+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NIN as Red List (low evidence)","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:32:34.162117+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nin has been classified as Red List (Low Evidence).","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:32:05.740837+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NIN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:31:49.181991+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NIN as Red List (low evidence)","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:31:49.167105+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nin has been classified as Red List (Low Evidence).","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:31:20.936425+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NIN: Rating: RED; Mode of pathogenicity: None; Publications: 22933543; Phenotypes: Seckel syndrome 7, MIM#614851; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:30:08.621543+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.870","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NIN: Rating: RED; Mode of pathogenicity: None; Publications: 22933543; Phenotypes: Seckel syndrome 7, MIM#614851; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NIN","entity_type":"gene"},{"created":"2019-12-08T07:22:43.936351+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.870","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NHLRC1 as ready","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2019-12-08T07:22:43.929474+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.870","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nhlrc1 has been classified as Red List (Low Evidence).","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2019-12-08T07:22:39.239960+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.870","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NHLRC1 were changed from  to Epilepsy, progressive myoclonic 2B (Lafora), MIM#254780","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2019-12-08T07:22:25.222478+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.869","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NHLRC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2019-12-08T07:22:18.686468+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.868","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NHLRC1 as Red List (low evidence)","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2019-12-08T07:22:18.678965+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.868","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nhlrc1 has been classified as Red List (Low Evidence).","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2019-12-08T07:22:02.219245+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.867","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NHLRC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Epilepsy, progressive myoclonic 2B (Lafora), MIM#254780; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NHLRC1","entity_type":"gene"},{"created":"2019-12-08T07:19:08.897419+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.867","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NFIB as ready","entity_name":"NFIB","entity_type":"gene"},{"created":"2019-12-08T07:19:08.889817+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.867","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfib has been classified as Green List (High Evidence).","entity_name":"NFIB","entity_type":"gene"},{"created":"2019-12-08T07:19:04.316829+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.867","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NFIB as Green List (high evidence)","entity_name":"NFIB","entity_type":"gene"},{"created":"2019-12-08T07:19:04.309260+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.867","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nfib has been classified as Green List (High Evidence).","entity_name":"NFIB","entity_type":"gene"},{"created":"2019-12-08T07:18:50.153791+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.866","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NFIB was added\ngene: NFIB was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list\nMode of inheritance for gene: NFIB was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NFIB were set to 30388402\nPhenotypes for gene: NFIB were set to Macrocephaly, acquired, with impaired intellectual development, MIM#618286\nReview for gene: NFIB was set to GREEN\nAdded comment: 18 individuals reported, of whom 11 had deletions of this gene and the rest had SNVs. \nSources: Expert list","entity_name":"NFIB","entity_type":"gene"},{"created":"2019-12-08T07:15:01.199132+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.865","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEGR1 as ready","entity_name":"NEGR1","entity_type":"gene"},{"created":"2019-12-08T07:15:01.191334+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.865","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: negr1 has been classified as Red List (Low Evidence).","entity_name":"NEGR1","entity_type":"gene"},{"created":"2019-12-08T07:14:52.520106+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.865","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NEGR1 as Red List (low evidence)","entity_name":"NEGR1","entity_type":"gene"},{"created":"2019-12-08T07:14:52.511414+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.865","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: negr1 has been classified as Red List (Low Evidence).","entity_name":"NEGR1","entity_type":"gene"},{"created":"2019-12-08T07:14:39.451902+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.864","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NEGR1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"NEGR1","entity_type":"gene"},{"created":"2019-12-08T07:11:02.209364+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.864","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEDD4L as ready","entity_name":"NEDD4L","entity_type":"gene"},{"created":"2019-12-08T07:11:02.198373+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.864","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nedd4l has been classified as Green List (High Evidence).","entity_name":"NEDD4L","entity_type":"gene"},{"created":"2019-12-08T07:10:57.807755+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.864","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NEDD4L were changed from  to Periventricular nodular heterotopia 7, MIM#617201","entity_name":"NEDD4L","entity_type":"gene"},{"created":"2019-12-08T07:10:40.281723+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.863","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NEDD4L was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NEDD4L","entity_type":"gene"},{"created":"2019-12-08T07:10:25.475281+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.862","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NEDD4L: Rating: GREEN; Mode of pathogenicity: None; Publications: 27694961; Phenotypes: Periventricular nodular heterotopia 7, MIM#617201; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NEDD4L","entity_type":"gene"},{"created":"2019-12-08T07:06:28.465231+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.193","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NECAP1 as ready","entity_name":"NECAP1","entity_type":"gene"},{"created":"2019-12-08T07:06:28.458302+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.193","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: necap1 has been classified as Amber List (Moderate Evidence).","entity_name":"NECAP1","entity_type":"gene"},{"created":"2019-12-08T07:06:20.471871+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.193","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NECAP1 were changed from  to Epileptic encephalopathy, early infantile, 21, MIM#615833","entity_name":"NECAP1","entity_type":"gene"},{"created":"2019-12-08T07:06:01.849404+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.192","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NECAP1 were set to ","entity_name":"NECAP1","entity_type":"gene"},{"created":"2019-12-08T07:05:39.835477+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.191","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NECAP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NECAP1","entity_type":"gene"},{"created":"2019-12-08T07:05:20.542791+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.190","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NECAP1 as Amber List (moderate evidence)","entity_name":"NECAP1","entity_type":"gene"},{"created":"2019-12-08T07:05:20.534544+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.190","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: necap1 has been classified as Amber List (Moderate Evidence).","entity_name":"NECAP1","entity_type":"gene"},{"created":"2019-12-08T07:04:38.717336+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.189","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EXT2 were changed from  to Seizures, scoliosis, and macrocephaly syndrome, MIM#616682","entity_name":"EXT2","entity_type":"gene"}]}