{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1921","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1919","results":[{"created":"2020-02-27T15:50:35.600611+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2232","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SOBP as Red List (low evidence)","entity_name":"SOBP","entity_type":"gene"},{"created":"2020-02-27T15:50:35.591875+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2232","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sobp has been classified as Red List (Low Evidence).","entity_name":"SOBP","entity_type":"gene"},{"created":"2020-02-27T15:50:04.479495+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2231","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SOBP: Rating: RED; Mode of pathogenicity: None; Publications: 21035105; Phenotypes: Mental retardation, anterior maxillary protrusion, and strabismus, MIM# 613671; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SOBP","entity_type":"gene"},{"created":"2020-02-27T14:51:58.814073+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2231","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SNORD118 as Amber List (moderate evidence)","entity_name":"SNORD118","entity_type":"gene"},{"created":"2020-02-27T14:51:58.800697+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2231","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snord118 has been classified as Amber List (Moderate Evidence).","entity_name":"SNORD118","entity_type":"gene"},{"created":"2020-02-27T14:51:26.126294+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2230","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SNORD118: Rating: AMBER; Mode of pathogenicity: None; Publications: 27571260; Phenotypes: Leukoencephalopathy, brain calcifications, and cysts, MIM# 614561; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SNORD118","entity_type":"gene"},{"created":"2020-02-27T14:43:18.216984+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SNIP1 as ready","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:43:18.207919+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snip1 has been classified as Red List (Low Evidence).","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:43:16.788705+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SNIP1 were changed from Psychomotor retardation, epilepsy, and craniofacial dysmorphism, 614501 to Psychomotor retardation, epilepsy, and craniofacial dysmorphism, 614501","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:42:57.760465+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SNIP1 were changed from  to Psychomotor retardation, epilepsy, and craniofacial dysmorphism, 614501","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:42:32.293384+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SNIP1 were set to ","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:42:08.490047+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SNIP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:41:40.222854+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SNIP1 as Red List (low evidence)","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:41:40.214420+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snip1 has been classified as Red List (Low Evidence).","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:41:10.702521+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SNIP1: Rating: RED; Mode of pathogenicity: None; Publications: 22279524; Phenotypes: Psychomotor retardation, epilepsy, and craniofacial dysmorphism, 614501; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:40:22.628752+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1467","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SNIP1 as ready","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:40:22.613869+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1467","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snip1 has been classified as Red List (Low Evidence).","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:40:09.654779+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1467","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SNIP1 were changed from  to Psychomotor retardation, epilepsy, and craniofacial dysmorphism, 614501","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:39:55.948668+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1466","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SNIP1 were set to ","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:39:40.855456+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1465","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SNIP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:39:20.728290+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1464","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SNIP1 as Red List (low evidence)","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:39:20.714972+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1464","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snip1 has been classified as Red List (Low Evidence).","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:38:23.580236+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1463","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SNIP1: Rating: RED; Mode of pathogenicity: None; Publications: 22279524; Phenotypes: Psychomotor retardation, epilepsy, and craniofacial dysmorphism, 614501; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:38:06.714325+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2230","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SNIP1 as ready","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:38:06.705565+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2230","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snip1 has been classified as Red List (Low Evidence).","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:35:39.126053+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2230","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SNIP1 were changed from Psychomotor retardation, epilepsy, and craniofacial dysmorphism, MIM# 614501 to Psychomotor retardation, epilepsy, and craniofacial dysmorphism, MIM# 614501","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:35:10.223351+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2229","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SNIP1 were changed from  to Psychomotor retardation, epilepsy, and craniofacial dysmorphism, MIM# 614501","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:34:48.869645+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2229","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SNIP1 were set to 22279524","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:34:27.902842+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2228","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SNIP1 were set to ","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:34:08.472572+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2228","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SNIP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:33:43.067487+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2227","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SNIP1 as Red List (low evidence)","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:33:43.054740+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2227","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snip1 has been classified as Red List (Low Evidence).","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:33:11.081901+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2226","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SNIP1: Rating: RED; Mode of pathogenicity: None; Publications: 22279524; Phenotypes: Psychomotor retardation, epilepsy, and craniofacial dysmorphism, MIM# 614501; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SNIP1","entity_type":"gene"},{"created":"2020-02-27T14:23:18.751810+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1463","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMG9 as ready","entity_name":"SMG9","entity_type":"gene"},{"created":"2020-02-27T14:23:18.738989+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1463","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smg9 has been classified as Green List (High Evidence).","entity_name":"SMG9","entity_type":"gene"},{"created":"2020-02-27T14:23:09.336076+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1463","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMG9 were changed from  to Heart and brain malformation syndrome, MIM# 616920","entity_name":"SMG9","entity_type":"gene"},{"created":"2020-02-27T14:22:47.855931+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1462","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMG9 were set to ","entity_name":"SMG9","entity_type":"gene"},{"created":"2020-02-27T14:22:27.392068+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1461","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMG9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMG9","entity_type":"gene"},{"created":"2020-02-27T14:22:07.576494+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1460","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMG9: Rating: GREEN; Mode of pathogenicity: None; Publications: 27018474, 31390136; Phenotypes: Heart and brain malformation syndrome, MIM# 616920; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMG9","entity_type":"gene"},{"created":"2020-02-27T14:20:43.384942+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2226","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMG9 as ready","entity_name":"SMG9","entity_type":"gene"},{"created":"2020-02-27T14:20:43.371287+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2226","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smg9 has been classified as Green List (High Evidence).","entity_name":"SMG9","entity_type":"gene"},{"created":"2020-02-27T14:20:36.761407+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2226","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SMG9 as Green List (high evidence)","entity_name":"SMG9","entity_type":"gene"},{"created":"2020-02-27T14:20:36.747352+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2226","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smg9 has been classified as Green List (High Evidence).","entity_name":"SMG9","entity_type":"gene"},{"created":"2020-02-27T14:20:03.064870+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2225","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SMG9 was added\ngene: SMG9 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list\nMode of inheritance for gene: SMG9 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SMG9 were set to 27018474; 31390136\nPhenotypes for gene: SMG9 were set to Heart and brain malformation syndrome, MIM#\t616920\nReview for gene: SMG9 was set to GREEN\nAdded comment: Three unrelated families reported, severe congenital malformation syndrome, ID is part of the phenotype in survivors. \nSources: Expert list","entity_name":"SMG9","entity_type":"gene"},{"created":"2020-02-27T14:04:44.545641+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2224","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMARCD2 as ready","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-02-27T14:04:44.531573+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2224","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarcd2 has been classified as Amber List (Moderate Evidence).","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-02-27T14:04:38.289795+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2224","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SMARCD2 as Amber List (moderate evidence)","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-02-27T14:04:38.276210+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2224","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarcd2 has been classified as Amber List (Moderate Evidence).","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-02-27T14:04:05.135946+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2223","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SMARCD2 was added\ngene: SMARCD2 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list\nMode of inheritance for gene: SMARCD2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SMARCD2 were set to 26350204; 28369036\nPhenotypes for gene: SMARCD2 were set to Specific granule deficiency 2, 617475 (includes global developmental delay in some patients)\nReview for gene: SMARCD2 was set to AMBER\nAdded comment: Candidate ID gene in PMID:26350204 and developmental delay seen in 2 patients with SGD2 PMID:28369036. \nSources: Expert list","entity_name":"SMARCD2","entity_type":"gene"},{"created":"2020-02-27T13:36:43.693528+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1460","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMPRSS3 as ready","entity_name":"TMPRSS3","entity_type":"gene"},{"created":"2020-02-27T13:36:43.685225+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1460","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmprss3 has been classified as Green List (High Evidence).","entity_name":"TMPRSS3","entity_type":"gene"},{"created":"2020-02-27T13:36:25.458574+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1460","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMPRSS3 were set to ","entity_name":"TMPRSS3","entity_type":"gene"},{"created":"2020-02-27T13:36:04.285218+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1459","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMPRSS3 were changed from  to Deafness, autosomal recessive 8/10, MIM#601072","entity_name":"TMPRSS3","entity_type":"gene"},{"created":"2020-02-27T13:35:20.271520+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1458","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMPRSS3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMPRSS3","entity_type":"gene"},{"created":"2020-02-27T13:35:00.605119+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1457","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TMPRSS3: Rating: GREEN; Mode of pathogenicity: None; Publications: 21786053, 17551081; Phenotypes: Deafness, autosomal recessive 8/10, MIM#601072; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMPRSS3","entity_type":"gene"},{"created":"2020-02-27T13:32:41.130600+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.325","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMPRSS3 as ready","entity_name":"TMPRSS3","entity_type":"gene"},{"created":"2020-02-27T13:32:41.115892+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.325","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmprss3 has been classified as Green List (High Evidence).","entity_name":"TMPRSS3","entity_type":"gene"},{"created":"2020-02-27T13:18:23.973855+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.325","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMPRSS3 were changed from  to Deafness, autosomal recessive 8/10, MIM#601072","entity_name":"TMPRSS3","entity_type":"gene"},{"created":"2020-02-27T13:18:01.848644+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.324","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMPRSS3 were set to ","entity_name":"TMPRSS3","entity_type":"gene"},{"created":"2020-02-27T13:17:39.485775+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.323","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMPRSS3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMPRSS3","entity_type":"gene"},{"created":"2020-02-27T13:16:59.882726+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.322","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GJB2 as ready","entity_name":"GJB2","entity_type":"gene"},{"created":"2020-02-27T13:16:59.868871+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.322","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gjb2 has been classified as Green List (High Evidence).","entity_name":"GJB2","entity_type":"gene"},{"created":"2020-02-27T13:16:56.587522+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.322","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GJB2 were changed from  to Bart-Pumphrey syndrome, MIM#149200; Deafness, autosomal dominant 3A, MIM#601544; Deafness, autosomal recessive 1A, MIM#220290; Hystrix-like ichthyosis with deafness, MIM#602540; Keratitis-ichthyosis-deafness syndrome, MIM#148210; Keratoderma, palmoplantar, with deafness, MIM#148350; Vohwinkel syndrome, MIM# 124500","entity_name":"GJB2","entity_type":"gene"},{"created":"2020-02-27T13:16:32.190976+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.321","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GJB2 were set to ","entity_name":"GJB2","entity_type":"gene"},{"created":"2020-02-27T13:16:08.726324+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.320","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GJB2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"GJB2","entity_type":"gene"},{"created":"2020-02-27T13:14:52.669724+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.319","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POU3F4 as ready","entity_name":"POU3F4","entity_type":"gene"},{"created":"2020-02-27T13:14:52.649106+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.319","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pou3f4 has been classified as Green List (High Evidence).","entity_name":"POU3F4","entity_type":"gene"},{"created":"2020-02-27T13:14:27.975250+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.319","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POU3F4 were changed from  to Deafness, X-linked 2, MIM# 304400","entity_name":"POU3F4","entity_type":"gene"},{"created":"2020-02-27T13:13:58.719863+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.318","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POU3F4 were set to ","entity_name":"POU3F4","entity_type":"gene"},{"created":"2020-02-27T13:13:29.404815+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.317","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: POU3F4 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"POU3F4","entity_type":"gene"},{"created":"2020-02-27T13:12:59.292783+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.316","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: POU3F4: Rating: GREEN; Mode of pathogenicity: None; Publications: 31786483, 30176854; Phenotypes: Deafness, X-linked 2, MIM# 304400; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"POU3F4","entity_type":"gene"},{"created":"2020-02-27T13:10:52.192422+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1457","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POU3F4 as ready","entity_name":"POU3F4","entity_type":"gene"},{"created":"2020-02-27T13:10:52.183156+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1457","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pou3f4 has been classified as Green List (High Evidence).","entity_name":"POU3F4","entity_type":"gene"},{"created":"2020-02-27T13:10:40.673722+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1457","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POU3F4 were changed from  to Deafness, X-linked 2, MIM#304400","entity_name":"POU3F4","entity_type":"gene"},{"created":"2020-02-27T13:09:53.087036+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1456","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POU3F4 were set to ","entity_name":"POU3F4","entity_type":"gene"},{"created":"2020-02-27T13:09:32.031578+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1455","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: POU3F4 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"POU3F4","entity_type":"gene"},{"created":"2020-02-27T13:08:27.146721+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.101","user_name":"Crystle Lee","item_type":"entity","text":"reviewed gene: COX4I2: Rating: RED; Mode of pathogenicity: Other; Publications: PMID: 19268275; Phenotypes: Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis (MIM#612714); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"COX4I2","entity_type":"gene"},{"created":"2020-02-27T13:08:26.544798+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1454","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLIT2 as ready","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:08:26.531176+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1454","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slit2 has been classified as Amber List (Moderate Evidence).","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:08:18.294645+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1454","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLIT2 were changed from  to CAKUT","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:08:00.056719+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1453","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLIT2 were set to ","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:07:40.320592+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1452","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLIT2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:07:22.008662+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1451","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLIT2 as Amber List (moderate evidence)","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:07:21.999817+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1451","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slit2 has been classified as Amber List (Moderate Evidence).","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:07:03.187592+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1450","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLIT2: Rating: AMBER; Mode of pathogenicity: None; Publications: 26026792, 15130495; Phenotypes: CAKUT; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:05:09.816393+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLIT2 as ready","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:05:09.807847+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slit2 has been classified as Red List (Low Evidence).","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:05:05.322070+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLIT2 were set to ","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:04:35.574760+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLIT2 as Red List (low evidence)","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:04:35.565020+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slit2 has been classified as Red List (Low Evidence).","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:03:35.514856+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLIT2: Rating: RED; Mode of pathogenicity: None; Publications: 22349628; Phenotypes: ; Mode of inheritance: None","entity_name":"SLIT2","entity_type":"gene"},{"created":"2020-02-27T13:01:39.569929+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FLT4 as ready","entity_name":"FLT4","entity_type":"gene"},{"created":"2020-02-27T13:01:39.560759+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: flt4 has been classified as Green List (High Evidence).","entity_name":"FLT4","entity_type":"gene"},{"created":"2020-02-27T13:01:34.720237+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FLT4 were changed from  to Congenital heart defects, multiple types, 7, MIM#618780","entity_name":"FLT4","entity_type":"gene"},{"created":"2020-02-27T13:00:48.079840+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FLT4 were set to ","entity_name":"FLT4","entity_type":"gene"},{"created":"2020-02-27T13:00:24.341924+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FLT4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FLT4","entity_type":"gene"},{"created":"2020-02-27T12:57:16.819554+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1450","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEL as ready","entity_name":"CEL","entity_type":"gene"},{"created":"2020-02-27T12:57:16.807326+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1450","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cel has been classified as Amber List (Moderate Evidence).","entity_name":"CEL","entity_type":"gene"},{"created":"2020-02-27T12:57:06.247180+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1450","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CEL were changed from  to Maturity-onset diabetes of the young, type VIII","entity_name":"CEL","entity_type":"gene"},{"created":"2020-02-27T12:56:45.502271+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1449","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CEL were set to ","entity_name":"CEL","entity_type":"gene"}]}