{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2080","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2078","results":[{"created":"2019-11-30T15:02:43.471741+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":"Marked gene: DISP1 as ready","entity_name":"DISP1","entity_type":"gene"},{"created":"2019-11-30T15:02:43.464592+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":"Gene: disp1 has been classified as Red List (Low Evidence).","entity_name":"DISP1","entity_type":"gene"},{"created":"2019-11-30T15:02:38.775826+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":"Phenotypes for gene: DISP1 were changed from  to Holoprosencephaly","entity_name":"DISP1","entity_type":"gene"},{"created":"2019-11-30T15:02:26.170614+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DISP1 were set to ","entity_name":"DISP1","entity_type":"gene"},{"created":"2019-11-30T15:02:11.319655+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DISP1 as Red List (low evidence)","entity_name":"DISP1","entity_type":"gene"},{"created":"2019-11-30T15:02:11.311957+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: disp1 has been classified as Red List (Low Evidence).","entity_name":"DISP1","entity_type":"gene"},{"created":"2019-11-30T15:01:58.886288+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DISP1: Rating: RED; Mode of pathogenicity: None; Publications: 19184110, 26748417, 23542665; Phenotypes: Holoprosencephaly; Mode of inheritance: Other","entity_name":"DISP1","entity_type":"gene"},{"created":"2019-11-30T14:55:25.499899+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DDX59 as ready","entity_name":"DDX59","entity_type":"gene"},{"created":"2019-11-30T14:55:25.492666+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ddx59 has been classified as Green List (High Evidence).","entity_name":"DDX59","entity_type":"gene"},{"created":"2019-11-30T14:55:21.133150+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DDX59 were changed from  to Orofaciodigital syndrome V, MIM#174300","entity_name":"DDX59","entity_type":"gene"},{"created":"2019-11-30T14:55:08.243245+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DDX59 were set to ","entity_name":"DDX59","entity_type":"gene"},{"created":"2019-11-30T14:54:51.308005+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: DDX59: Some affected individuals are reported as having ID.","entity_name":"DDX59","entity_type":"gene"},{"created":"2019-11-30T14:51:25.536799+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DDX59: Rating: GREEN; Mode of pathogenicity: None; Publications: 28711741, 23972372, 29127725; Phenotypes: Orofaciodigital syndrome V, MIM#174300; Mode of inheritance: None","entity_name":"DDX59","entity_type":"gene"},{"created":"2019-11-30T14:47:18.594665+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DDR2 as ready","entity_name":"DDR2","entity_type":"gene"},{"created":"2019-11-30T14:47:18.587035+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ddr2 has been classified as Red List (Low Evidence).","entity_name":"DDR2","entity_type":"gene"},{"created":"2019-11-30T14:47:12.662806+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DDR2 were changed from  to Warburg-Cinotti syndrome, MIM#618175, AD; Spondylometaepiphyseal dysplasia, short limb-hand type, MIM#271665, AR","entity_name":"DDR2","entity_type":"gene"},{"created":"2019-11-30T14:46:57.947584+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DDR2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"DDR2","entity_type":"gene"},{"created":"2019-11-30T14:46:50.952842+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DDR2 as Red List (low evidence)","entity_name":"DDR2","entity_type":"gene"},{"created":"2019-11-30T14:46:50.945280+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ddr2 has been classified as Red List (Low Evidence).","entity_name":"DDR2","entity_type":"gene"},{"created":"2019-11-30T14:46:37.160233+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DDR2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Warburg-Cinotti syndrome, MIM#618175, AD, Spondylometaepiphyseal dysplasia, short limb-hand type, MIM#271665, AR; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"DDR2","entity_type":"gene"},{"created":"2019-11-30T14:42:42.651713+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DDB1 as ready","entity_name":"DDB1","entity_type":"gene"},{"created":"2019-11-30T14:42:42.644540+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ddb1 has been classified as Green List (High Evidence).","entity_name":"DDB1","entity_type":"gene"},{"created":"2019-11-30T14:42:37.092788+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DDB1 as Green List (high evidence)","entity_name":"DDB1","entity_type":"gene"},{"created":"2019-11-30T14:42:37.085708+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ddb1 has been classified as Green List (High Evidence).","entity_name":"DDB1","entity_type":"gene"},{"created":"2019-11-30T14:42:24.379750+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DDB1 was added\ngene: DDB1 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Research\nMode of inheritance for gene: DDB1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: DDB1 were set to Syndromic intellectual disability\nReview for gene: DDB1 was set to GREEN\nAdded comment: High quality unpublished evidence. \nSources: Research","entity_name":"DDB1","entity_type":"gene"},{"created":"2019-11-30T14:40:44.442988+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DDB1 as ready","entity_name":"DDB1","entity_type":"gene"},{"created":"2019-11-30T14:40:44.435460+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ddb1 has been classified as Green List (High Evidence).","entity_name":"DDB1","entity_type":"gene"},{"created":"2019-11-30T14:40:31.884370+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DDB1 were changed from  to Syndromic intellectual disability","entity_name":"DDB1","entity_type":"gene"},{"created":"2019-11-30T14:40:17.347553+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DDB1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DDB1","entity_type":"gene"},{"created":"2019-11-30T14:39:57.393054+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DDB1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Syndromic intellectual disability; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DDB1","entity_type":"gene"},{"created":"2019-11-30T14:34:57.398027+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CNTN4 as ready","entity_name":"CNTN4","entity_type":"gene"},{"created":"2019-11-30T14:34:57.390002+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cntn4 has been classified as Red List (Low Evidence).","entity_name":"CNTN4","entity_type":"gene"},{"created":"2019-11-30T14:34:51.358677+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CNTN4 were changed from  to Intellectual disability; SCA","entity_name":"CNTN4","entity_type":"gene"},{"created":"2019-11-30T14:34:38.094162+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CNTN4 were set to ","entity_name":"CNTN4","entity_type":"gene"},{"created":"2019-11-30T14:34:20.751704+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CNTN4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CNTN4","entity_type":"gene"},{"created":"2019-11-30T14:34:14.073958+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CNTN4 as Red List (low evidence)","entity_name":"CNTN4","entity_type":"gene"},{"created":"2019-11-30T14:34:14.063536+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cntn4 has been classified as Red List (Low Evidence).","entity_name":"CNTN4","entity_type":"gene"},{"created":"2019-11-30T12:59:03.740220+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYP2U1 as ready","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2019-11-30T12:59:03.733050+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyp2u1 has been classified as Red List (Low Evidence).","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2019-11-30T12:58:56.411569+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CYP2U1 were changed from  to Spastic paraplegia 56, autosomal recessive, MIM#615030","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2019-11-30T12:58:49.284604+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CYP2U1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2019-11-30T12:58:32.871180+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CYP2U1 as Red List (low evidence)","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2019-11-30T12:58:32.862771+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyp2u1 has been classified as Red List (Low Evidence).","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2019-11-30T12:58:18.744579+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CYP2U1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Spastic paraplegia 56, autosomal recessive, MIM#615030; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CYP2U1","entity_type":"gene"},{"created":"2019-11-30T12:01:32.659611+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CYFIP1 as ready","entity_name":"CYFIP1","entity_type":"gene"},{"created":"2019-11-30T12:01:32.652459+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyfip1 has been classified as Red List (Low Evidence).","entity_name":"CYFIP1","entity_type":"gene"},{"created":"2019-11-30T12:01:25.059034+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CYFIP1 as Red List (low evidence)","entity_name":"CYFIP1","entity_type":"gene"},{"created":"2019-11-30T12:01:25.051166+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cyfip1 has been classified as Red List (Low Evidence).","entity_name":"CYFIP1","entity_type":"gene"},{"created":"2019-11-30T12:01:09.875513+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CYFIP1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"CYFIP1","entity_type":"gene"},{"created":"2019-11-30T11:56:00.947891+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CUX2 as ready","entity_name":"CUX2","entity_type":"gene"},{"created":"2019-11-30T11:56:00.938970+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cux2 has been classified as Green List (High Evidence).","entity_name":"CUX2","entity_type":"gene"},{"created":"2019-11-30T11:55:39.792141+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CUX2 were changed from  to Epileptic encephalopathy, early infantile, 67, MIM#618141","entity_name":"CUX2","entity_type":"gene"},{"created":"2019-11-30T11:55:17.397850+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CUX2 were set to ","entity_name":"CUX2","entity_type":"gene"},{"created":"2019-11-30T11:54:32.979086+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CUX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CUX2","entity_type":"gene"},{"created":"2019-11-30T11:53:24.749104+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CUX2: Rating: GREEN; Mode of pathogenicity: None; Publications: 29630738, 29795476; Phenotypes: Epileptic encephalopathy, early infantile, 67, MIM#618141; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CUX2","entity_type":"gene"},{"created":"2019-11-30T11:50:43.441124+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CUBN as ready","entity_name":"CUBN","entity_type":"gene"},{"created":"2019-11-30T11:50:43.433204+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cubn has been classified as Red List (Low Evidence).","entity_name":"CUBN","entity_type":"gene"},{"created":"2019-11-30T11:50:37.016387+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CUBN were changed from  to Megaloblastic anemia-1, Finnish type, MIM#261100; Proteinuria","entity_name":"CUBN","entity_type":"gene"},{"created":"2019-11-30T11:50:18.398213+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CUBN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CUBN","entity_type":"gene"},{"created":"2019-11-30T11:50:00.125785+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CUBN as Red List (low evidence)","entity_name":"CUBN","entity_type":"gene"},{"created":"2019-11-30T11:50:00.117610+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cubn has been classified as Red List (Low Evidence).","entity_name":"CUBN","entity_type":"gene"},{"created":"2019-11-30T11:49:48.136916+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CUBN: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Megaloblastic anemia-1, Finnish type, MIM#261100, Proteinuria; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CUBN","entity_type":"gene"},{"created":"2019-11-30T11:47:43.342355+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTU2 as ready","entity_name":"CTU2","entity_type":"gene"},{"created":"2019-11-30T11:47:43.334719+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctu2 has been classified as Green List (High Evidence).","entity_name":"CTU2","entity_type":"gene"},{"created":"2019-11-30T11:47:34.385752+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CTU2 as Green List (high evidence)","entity_name":"CTU2","entity_type":"gene"},{"created":"2019-11-30T11:47:34.378296+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctu2 has been classified as Green List (High Evidence).","entity_name":"CTU2","entity_type":"gene"},{"created":"2019-11-30T11:47:19.029780+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CTU2 was added\ngene: CTU2 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list\nMode of inheritance for gene: CTU2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CTU2 were set to 27480277; 26633546\nPhenotypes for gene: CTU2 were set to Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome, MIM#618142\nReview for gene: CTU2 was set to GREEN\nAdded comment: Multiple Saudi families reported with same homozygous variant; founder effect. Severe disorder of infancy. \nSources: Expert list","entity_name":"CTU2","entity_type":"gene"},{"created":"2019-11-30T11:41:00.302153+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTSF as ready","entity_name":"CTSF","entity_type":"gene"},{"created":"2019-11-30T11:41:00.294621+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctsf has been classified as Red List (Low Evidence).","entity_name":"CTSF","entity_type":"gene"},{"created":"2019-11-30T11:40:44.819596+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTSF were changed from  to Ceroid lipofuscinosis, neuronal, 13, Kufs type, MIM#615362","entity_name":"CTSF","entity_type":"gene"},{"created":"2019-11-30T11:40:37.813613+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTSF was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTSF","entity_type":"gene"},{"created":"2019-11-30T11:40:21.528935+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CTSF as Red List (low evidence)","entity_name":"CTSF","entity_type":"gene"},{"created":"2019-11-30T11:40:21.520210+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctsf has been classified as Red List (Low Evidence).","entity_name":"CTSF","entity_type":"gene"},{"created":"2019-11-30T11:40:07.451506+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTSF: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ceroid lipofuscinosis, neuronal, 13, Kufs type, MIM#615362; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTSF","entity_type":"gene"},{"created":"2019-11-30T11:37:00.552152+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNNA2 as ready","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:37:00.544298+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnna2 has been classified as Green List (High Evidence).","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:36:56.236791+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNNA2 were changed from  to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:36:34.421178+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTNNA2 were set to ","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:36:19.975541+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNNA2 were changed from Cortical dysplasia, complex, with other brain malformations 9, MIM#618174 to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:36:09.174968+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNNA2 as ready","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:36:09.166256+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnna2 has been classified as Green List (High Evidence).","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:36:00.407398+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNNA2 were changed from Cortical dysplasia, complex, with other brain malformations 9, MIM#618174 to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:35:42.879593+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNNA2 were changed from  to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:35:27.458863+11:00","panel_name":"Callosome_VCGS","panel_id":205,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTNNA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:35:08.264504+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTNNA2 were set to ","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:34:34.970665+11:00","panel_name":"Microcephaly_VCGS","panel_id":138,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTNNA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:34:34.627373+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNNA2 as ready","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:34:34.603588+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnna2 has been classified as Green List (High Evidence).","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:33:59.979991+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNNA2 were changed from  to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:33:44.373160+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTNNA2 were set to ","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:33:27.942969+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTNNA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:29:28.308028+11:00","panel_name":"Lissencephaly and band heterotopia_AustralianGenomics_VCGS","panel_id":15,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNNA2 as ready","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:29:28.300883+11:00","panel_name":"Lissencephaly and band heterotopia_AustralianGenomics_VCGS","panel_id":15,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnna2 has been classified as Green List (High Evidence).","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:29:22.081459+11:00","panel_name":"Lissencephaly and band heterotopia_AustralianGenomics_VCGS","panel_id":15,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNNA2 were changed from  to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:29:02.131603+11:00","panel_name":"Lissencephaly and band heterotopia_AustralianGenomics_VCGS","panel_id":15,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTNNA2 were set to ","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:28:35.351367+11:00","panel_name":"Lissencephaly and band heterotopia_AustralianGenomics_VCGS","panel_id":15,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTNNA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:28:07.958975+11:00","panel_name":"Lissencephaly and band heterotopia_AustralianGenomics_VCGS","panel_id":15,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTNNA2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30013181; Phenotypes: Cortical dysplasia, complex, with other brain malformations 9, MIM#618174; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:26:15.599274+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNNA2 as ready","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:26:15.584624+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnna2 has been classified as Green List (High Evidence).","entity_name":"CTNNA2","entity_type":"gene"},{"created":"2019-11-30T11:26:14.934069+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ","panel_id":250,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CTNNA2 as Green List (high evidence)","entity_name":"CTNNA2","entity_type":"gene"}]}