{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1117","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1115","results":[{"created":"2021-11-26T09:24:51.073887+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.734","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CUL4B were set to ","entity_name":"CUL4B","entity_type":"gene"},{"created":"2021-11-26T09:24:36.438934+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.733","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CUL4B: Rating: GREEN; Mode of pathogenicity: None; Publications: 17236139, 19377476; Phenotypes: Mental retardation, X-linked, syndromic 15 (Cabezas type), MIM# 300354; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"CUL4B","entity_type":"gene"},{"created":"2021-11-26T09:22:00.408468+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9888","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTSK as ready","entity_name":"CTSK","entity_type":"gene"},{"created":"2021-11-26T09:22:00.395976+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9888","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctsk has been classified as Green List (High Evidence).","entity_name":"CTSK","entity_type":"gene"},{"created":"2021-11-26T09:21:42.237672+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9888","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTSK were changed from  to Pycnodysostosis, MIM# 265800","entity_name":"CTSK","entity_type":"gene"},{"created":"2021-11-26T09:21:20.233063+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9887","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTSK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTSK","entity_type":"gene"},{"created":"2021-11-26T09:21:03.107330+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9886","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTSK: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pycnodysostosis, MIM# 265800; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTSK","entity_type":"gene"},{"created":"2021-11-26T09:20:16.294931+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.733","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTSK as ready","entity_name":"CTSK","entity_type":"gene"},{"created":"2021-11-26T09:20:16.284866+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.733","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctsk has been classified as Green List (High Evidence).","entity_name":"CTSK","entity_type":"gene"},{"created":"2021-11-26T09:20:12.250712+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.733","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTSK were changed from PYCNODYSOSTOSIS to Pycnodysostosis, MIM# 265800","entity_name":"CTSK","entity_type":"gene"},{"created":"2021-11-26T09:19:56.146669+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.732","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTSK: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pycnodysostosis, MIM# 265800; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTSK","entity_type":"gene"},{"created":"2021-11-26T09:17:06.990444+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.732","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTSD as ready","entity_name":"CTSD","entity_type":"gene"},{"created":"2021-11-26T09:17:06.980118+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.732","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctsd has been classified as Green List (High Evidence).","entity_name":"CTSD","entity_type":"gene"},{"created":"2021-11-26T09:17:01.679922+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.732","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTSD were changed from NEURONAL CEROID LIPOFUSCINOSIS TYPE 10 to Ceroid lipofuscinosis, neuronal, 10, MIM# 610127","entity_name":"CTSD","entity_type":"gene"},{"created":"2021-11-26T09:16:40.166578+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.731","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTSD were set to ","entity_name":"CTSD","entity_type":"gene"},{"created":"2021-11-26T09:16:24.173433+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.730","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTSD: Rating: GREEN; Mode of pathogenicity: None; Publications: 1558577; Phenotypes: Ceroid lipofuscinosis, neuronal, 10, MIM# 610127; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTSD","entity_type":"gene"},{"created":"2021-11-26T09:11:28.012808+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.729","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTSA as ready","entity_name":"CTSA","entity_type":"gene"},{"created":"2021-11-26T09:11:28.002113+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.729","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctsa has been classified as Green List (High Evidence).","entity_name":"CTSA","entity_type":"gene"},{"created":"2021-11-26T09:11:07.487832+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.729","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTSA were changed from GALACTOSIALIDOSIS to Galactosialidosis, MIM# 256540","entity_name":"CTSA","entity_type":"gene"},{"created":"2021-11-26T09:10:49.477099+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.728","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTSA: Rating: GREEN; Mode of pathogenicity: None; Publications: 7759227; Phenotypes: Galactosialidosis, MIM# 256540; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CTSA","entity_type":"gene"},{"created":"2021-11-26T09:02:38.342658+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4307","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNNB1 as ready","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T09:02:38.330400+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4307","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnnb1 has been classified as Green List (High Evidence).","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T09:02:24.392335+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4307","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNNB1 were changed from  to Neurodevelopmental disorder with spastic diplegia and visual defects , MIM#615075","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T09:01:53.969524+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4306","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTNNB1 were set to ","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T09:00:47.949681+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4305","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTNNB1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T09:00:15.017416+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4304","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTNNB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23033978, 24614104, 25326669, 27915094; Phenotypes: Neurodevelopmental disorder with spastic diplegia and visual defects , MIM#615075; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T08:59:11.118328+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.728","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNNB1 as ready","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T08:59:11.107889+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.728","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnnb1 has been classified as Green List (High Evidence).","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T08:59:07.510981+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.728","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNNB1 were changed from MENTAL RETARDATION, AUTOSOMAL DOMINANT 19 to Neurodevelopmental disorder with spastic diplegia and visual defects , MIM#615075","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T08:58:54.992596+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.727","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTNNB1 were set to 27915094","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T08:58:40.231416+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.726","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTNNB1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T08:58:26.655498+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.725","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTNNB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23033978, 24614104, 25326669, 27915094; Phenotypes: Neurodevelopmental disorder with spastic diplegia and visual defects , MIM#615075; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-11-26T08:55:31.510516+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTCF as ready","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:55:31.500209+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctcf has been classified as Green List (High Evidence).","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:55:28.318947+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTCF were changed from MENTAL RETARDATION, AUTOSOMAL DOMINANT 21; MRD21 to Mental retardation, autosomal dominant 21 (MIM#615502)","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:55:14.973544+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTCF were set to ","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:55:06.615866+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.149","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTCF was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:54:55.703666+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTCF: Rating: GREEN; Mode of pathogenicity: None; Publications: 23746550, 31239556; Phenotypes: Mental retardation, autosomal dominant 21 (MIM#615502); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:53:59.187533+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9886","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTCF as ready","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:53:59.176443+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9886","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctcf has been classified as Green List (High Evidence).","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:53:50.827905+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9886","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTCF were changed from  to Mental retardation, autosomal dominant 21 (MIM#615502)","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:53:31.910378+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9885","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTCF were set to ","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:53:08.553580+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9884","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTCF was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:52:49.908990+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9883","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTCF: Rating: GREEN; Mode of pathogenicity: None; Publications: 23746550, 31239556; Phenotypes: Mental retardation, autosomal dominant 21 (MIM#615502); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:51:37.110363+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.725","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTCF as ready","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:51:37.099610+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.725","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctcf has been classified as Green List (High Evidence).","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:51:33.449072+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.725","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTCF were changed from INTELLECTUAL DISABILITY to Mental retardation, autosomal dominant 21 (MIM#615502)","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:51:20.572695+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.724","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTCF were set to ","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:51:03.908734+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.723","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTCF: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation, autosomal dominant 21 (MIM#615502); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:49:27.309423+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.723","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTCF was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTCF","entity_type":"gene"},{"created":"2021-11-26T08:44:15.038228+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.722","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTC1 as ready","entity_name":"CTC1","entity_type":"gene"},{"created":"2021-11-26T08:44:15.027516+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.722","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctc1 has been classified as Green List (High Evidence).","entity_name":"CTC1","entity_type":"gene"},{"created":"2021-11-26T08:44:10.641956+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.722","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTC1 were changed from CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS to Cerebroretinal microangiopathy with calcifications and cysts, MIM# 612199","entity_name":"CTC1","entity_type":"gene"},{"created":"2021-11-26T08:43:58.924937+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.721","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTC1 were set to ","entity_name":"CTC1","entity_type":"gene"},{"created":"2021-11-26T08:43:44.957696+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.720","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"CTC1","entity_type":"gene"},{"created":"2021-11-26T08:43:41.121030+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.720","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: CTC1: Added comment: Cerebroretinal microangiopathy with calcifications and cysts (CRMCC), also known as Coats plus syndrome, is an autosomal recessive pleomorphic disorder characterized primarily by intracranial calcifications, leukodystrophy, and brain cysts, resulting in spasticity, ataxia, dystonia, seizures, and cognitive decline. Patients also have retinal telangiectasia and exudates (Coats disease) as well as extraneurologic manifestations, including osteopenia with poor bone healing and a high risk of gastrointestinal bleeding and portal hypertension caused by vasculature ectasias in the stomach, small intestine, and liver. Some individuals also have hair, skin, and nail changes, as well as anaemia and thrombocytopaenia.\r\n\r\nMultiple families reported.; Changed rating: GREEN; Changed publications: 22267198","entity_name":"CTC1","entity_type":"gene"},{"created":"2021-11-26T08:41:56.249988+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.720","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CSPP1 as ready","entity_name":"CSPP1","entity_type":"gene"},{"created":"2021-11-26T08:41:56.239157+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.720","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cspp1 has been classified as Green List (High Evidence).","entity_name":"CSPP1","entity_type":"gene"},{"created":"2021-11-26T08:41:51.600284+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.720","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CSPP1 were changed from JOUBERT SYNDROME WITH OR WITHOUT JEUNE ASPHYXIATING THORACIC DYSTROPHY to Joubert syndrome 21, MIM# 615636; MONDO:0014288","entity_name":"CSPP1","entity_type":"gene"},{"created":"2021-11-26T08:41:10.750052+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.719","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CSPP1 were set to ","entity_name":"CSPP1","entity_type":"gene"},{"created":"2021-11-26T08:40:38.538814+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4304","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CSNK2A1 as ready","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:40:38.525832+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4304","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: csnk2a1 has been classified as Green List (High Evidence).","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:40:31.938409+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4304","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CSNK2A1 were changed from  to Okur-Chung neurodevelopmental syndrome, MIM# 617062","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:39:54.285984+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4303","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CSNK2A1 were set to ","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:39:25.244068+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4302","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CSNK2A1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:38:50.673148+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4301","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CSNK2A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27048600, 29240241, 29383814; Phenotypes: Okur-Chung neurodevelopmental syndrome, MIM# 617062; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:38:13.455401+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9883","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CSNK2A1 as ready","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:38:13.445649+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9883","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: csnk2a1 has been classified as Green List (High Evidence).","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:37:59.100414+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9883","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CSNK2A1 were changed from  to Okur-Chung neurodevelopmental syndrome, MIM# 617062","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:37:38.637399+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9882","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CSNK2A1 were set to ","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:37:20.496238+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9881","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CSNK2A1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:37:01.415270+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9880","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CSNK2A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27048600, 29240241, 29383814; Phenotypes: Okur-Chung neurodevelopmental syndrome, MIM# 617062; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:36:11.292748+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.718","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CSNK2A1 as ready","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:36:11.282224+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.718","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: csnk2a1 has been classified as Green List (High Evidence).","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:36:07.525541+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.718","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CSNK2A1 were changed from CSNK2A1 syndrome; Okur-Chung neurodevelopmental syndrome, 617062 to Okur-Chung neurodevelopmental syndrome, MIM# 617062","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:35:54.882166+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.717","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CSNK2A1 were set to ","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:35:42.904897+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.716","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CSNK2A1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-26T08:35:31.094387+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.715","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CSNK2A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27048600, 29240241, 29383814; Phenotypes: Okur-Chung neurodevelopmental syndrome, MIM# 617062; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CSNK2A1","entity_type":"gene"},{"created":"2021-11-25T19:57:57.510132+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.319","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYGD as ready","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:57:57.499061+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.319","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crygd has been classified as Green List (High Evidence).","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:57:52.408120+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.319","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYGD were changed from  to Cataract 4, multiple types, MIM# 115700","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:57:18.371284+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.318","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYGD were set to ","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:56:54.272119+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.317","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYGD was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:56:24.449866+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.316","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYGD: Rating: GREEN; Mode of pathogenicity: None; Publications: 9927684, 10915766, 12676897, 17724170; Phenotypes: Cataract 4, multiple types, MIM# 115700; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:55:43.841502+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9880","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYGD as ready","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:55:43.832125+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9880","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crygd has been classified as Green List (High Evidence).","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:55:35.878002+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9880","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYGD were changed from  to Cataract 4, multiple types, MIM# 115700","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:55:16.184456+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9879","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYGD were set to ","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:54:57.620552+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9878","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYGD was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:54:39.338658+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.9877","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYGD: Rating: GREEN; Mode of pathogenicity: None; Publications: 9927684, 10915766, 12676897, 17724170; Phenotypes: Cataract 4, multiple types, MIM# 115700; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:53:47.314092+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.715","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYGD as ready","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:53:47.303155+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.715","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crygd has been classified as Green List (High Evidence).","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:46:10.696503+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.715","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYGD were changed from CATARACT AUTOSOMAL DOMINANT; CATARACT CONGENITAL CERULEAN TYPE 3 to Cataract 4, multiple types, MIM# 115700","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:01:49.824984+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.714","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYGD were set to ","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:01:12.145221+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.713","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYGD was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T19:00:55.901698+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.712","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CRYGD: Rating: GREEN; Mode of pathogenicity: None; Publications: 9927684, 10915766, 12676897, 17724170; Phenotypes: Cataract 4, multiple types, MIM# 115700; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYGD","entity_type":"gene"},{"created":"2021-11-25T18:10:11.251480+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.316","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYGC as ready","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:10:11.240785+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.316","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crygc has been classified as Green List (High Evidence).","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:10:08.905578+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.316","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYGC were changed from  to Cataract 2, multiple types, MIM# 604307","entity_name":"CRYGC","entity_type":"gene"},{"created":"2021-11-25T18:09:38.831774+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.315","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYGC were set to ","entity_name":"CRYGC","entity_type":"gene"}]}