{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1308","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1306","results":[{"created":"2021-06-06T10:02:31.500552+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3818","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MASP1 were changed from  to 3MC syndrome 1, MIM# 257920; MONDO:0009770","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T10:02:04.564588+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3817","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MASP1 were set to ","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T10:01:31.089223+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3816","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MASP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T10:00:59.832429+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3815","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MASP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26789649, 21258343, 21035106; Phenotypes: 3MC syndrome 1, MIM# 257920, MONDO:0009770; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T10:00:19.200534+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7863","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MASP1 as ready","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T10:00:19.187085+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7863","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: masp1 has been classified as Green List (High Evidence).","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T10:00:08.234560+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7863","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MASP1 were changed from  to 3MC syndrome 1, MIM# 257920; MONDO:0009770","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T09:59:49.746732+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7862","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MASP1 were set to ","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T09:59:29.354605+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7861","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MASP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T09:59:12.858690+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7860","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MASP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26789649, 21258343, 21035106; Phenotypes: 3MC syndrome 1, MIM# 257920, MONDO:0009770; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T09:58:22.253359+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MASP1 as ready","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T09:58:22.243912+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: masp1 has been classified as Green List (High Evidence).","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T09:58:18.700405+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MASP1 were changed from  to 3MC syndrome 1, MIM# 257920; MONDO:0009770","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T09:57:50.299109+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MASP1 were set to ","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T09:57:20.836741+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MASP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T09:56:52.529064+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MASP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26789649, 21258343, 21035106; Phenotypes: 3MC syndrome 1, MIM# 257920, MONDO:0009770; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MASP1","entity_type":"gene"},{"created":"2021-06-06T09:52:55.498613+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KAT6B as ready","entity_name":"KAT6B","entity_type":"gene"},{"created":"2021-06-06T09:52:55.485651+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kat6b has been classified as Green List (High Evidence).","entity_name":"KAT6B","entity_type":"gene"},{"created":"2021-06-06T09:52:51.095453+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KAT6B were changed from SBBYSS syndrome, MIM# 603736; MONDO:0011365 to SBBYSS syndrome, MIM# 603736; MONDO:0011365","entity_name":"KAT6B","entity_type":"gene"},{"created":"2021-06-06T09:52:36.299593+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KAT6B were changed from  to SBBYSS syndrome, MIM# 603736; MONDO:0011365","entity_name":"KAT6B","entity_type":"gene"},{"created":"2021-06-06T09:52:08.338923+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KAT6B were set to ","entity_name":"KAT6B","entity_type":"gene"},{"created":"2021-06-06T09:51:42.103125+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KAT6B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KAT6B","entity_type":"gene"},{"created":"2021-06-06T09:51:18.426922+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KAT6B: Rating: GREEN; Mode of pathogenicity: None; Publications: 32424177; Phenotypes: SBBYSS syndrome, MIM# 603736, MONDO:0011365; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KAT6B","entity_type":"gene"},{"created":"2021-06-06T09:48:31.066388+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3815","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRPF1 as ready","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:48:31.054628+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3815","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brpf1 has been classified as Green List (High Evidence).","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:48:26.816092+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3815","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BRPF1 were changed from  to Intellectual developmental disorder with dysmorphic facies and ptosis, MIM# 617333; MONDO:0015022","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:47:52.562548+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3814","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BRPF1 were set to ","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:47:27.095959+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3813","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BRPF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:46:52.747048+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3812","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BRPF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27939640, 27939639, 32652122; Phenotypes: Intellectual developmental disorder with dysmorphic facies and ptosis, MIM# 617333, MONDO:0015022; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:46:06.605666+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7860","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRPF1 as ready","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:46:06.595957+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7860","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brpf1 has been classified as Green List (High Evidence).","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:45:57.034940+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7860","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BRPF1 were changed from  to Intellectual developmental disorder with dysmorphic facies and ptosis, MIM# 617333; MONDO:0015022","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:45:42.189750+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7859","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BRPF1 were set to ","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:45:20.170925+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7858","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BRPF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:45:04.154070+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7857","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BRPF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27939640, 27939639; Phenotypes: Intellectual developmental disorder with dysmorphic facies and ptosis, MIM# 617333, MONDO:0015022; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:44:06.815119+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRPF1 as ready","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:44:06.805264+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brpf1 has been classified as Green List (High Evidence).","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:43:58.959296+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BRPF1 as Green List (high evidence)","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:43:58.948891+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brpf1 has been classified as Green List (High Evidence).","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-06T09:43:35.231354+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BRPF1 was added\ngene: BRPF1 was added to Blepharophimosis. Sources: Expert Review\nMode of inheritance for gene: BRPF1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: BRPF1 were set to 27939640; 27939639\nPhenotypes for gene: BRPF1 were set to Intellectual developmental disorder with dysmorphic facies and ptosis, MIM#\t617333; MONDO:0015022\nReview for gene: BRPF1 was set to GREEN\nAdded comment: Intellectual developmental disorder with dysmorphic facies and ptosis is an autosomal dominant neurodevelopmental disorder characterized by delayed psychomotor development, intellectual disability, delayed language, and dysmorphic facial features, most notably ptosis/blepharophimosis. Additional features may include poor growth, hypotonia, and seizures.\r\n\r\nAt least 10 unrelated families reported. \nSources: Expert Review","entity_name":"BRPF1","entity_type":"gene"},{"created":"2021-06-05T19:21:43.310047+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3812","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POGZ as ready","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:21:43.301086+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3812","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pogz has been classified as Green List (High Evidence).","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:21:35.376800+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3812","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POGZ were changed from  to White-Sutton syndrome, MIM# 616364; MONDO:0014606","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:21:08.772042+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3811","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POGZ were set to ","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:18:07.759779+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3810","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: POGZ was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:17:40.431144+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3809","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: POGZ: Rating: GREEN; Mode of pathogenicity: None; Publications: 33098347, 31782611, 26942287; Phenotypes: White-Sutton syndrome, MIM# 616364, MONDO:0014606; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:17:29.199460+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POGZ were changed from  to White-Sutton syndrome, MIM# 616364; MONDO:0014606","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:16:57.001584+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POGZ were set to ","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:16:35.602265+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: POGZ was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:16:05.363009+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: POGZ as Amber List (moderate evidence)","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:16:05.352442+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pogz has been classified as Amber List (Moderate Evidence).","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:15:41.043666+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: POGZ: Rating: AMBER; Mode of pathogenicity: None; Publications: 33098347, 31782611, 26942287; Phenotypes: White-Sutton syndrome, MIM# 616364, MONDO:0014606; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"POGZ","entity_type":"gene"},{"created":"2021-06-05T19:07:06.859081+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAF7 as ready","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T19:07:06.849886+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: traf7 has been classified as Green List (High Evidence).","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T19:07:02.768337+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRAF7 as Green List (high evidence)","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T19:07:02.758723+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: traf7 has been classified as Green List (High Evidence).","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:41:04.716882+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRAF7 was added\ngene: TRAF7 was added to Congenital Heart Defect. Sources: Expert Review\nMode of inheritance for gene: TRAF7 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: TRAF7 were set to 32376980\nPhenotypes for gene: TRAF7 were set to Cardiac, facial, and digital anomalies with developmental delay, MIM# 618164\nReview for gene: TRAF7 was set to GREEN\nAdded comment: More than 40 individuals reported with DD/ID and a recognizable facial gestalt (characterized in particular by blepharophimosis), short neck, pectus carinatum, digital deviations and patent ductus arteriosus. Almost all variants occur in the WD40 repeats and most are recurrent. \nSources: Expert Review","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:39:36.304466+10:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAF7 as ready","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:39:36.293823+10:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: traf7 has been classified as Green List (High Evidence).","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:39:33.781767+10:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRAF7 were changed from  to Cardiac, facial, and digital anomalies with developmental delay, MIM# 618164","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:39:04.283780+10:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAF7 were set to ","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:37:35.062638+10:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRAF7 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:37:03.701284+10:00","panel_name":"Macrocephaly_Megalencephaly","panel_id":135,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRAF7: Rating: GREEN; Mode of pathogenicity: None; Publications: 32376980; Phenotypes: Cardiac, facial, and digital anomalies with developmental delay, MIM# 618164; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:34:32.496045+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.75","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAF7 were set to 29961569","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:34:10.315428+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.74","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TRAF7 as Green List (high evidence)","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:34:10.305520+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.74","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: traf7 has been classified as Green List (High Evidence).","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:33:42.099271+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.73","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRAF7: Rating: GREEN; Mode of pathogenicity: None; Publications: 32376980; Phenotypes: Cardiac, facial, and digital anomalies with developmental delay, MIM# 618164; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:32:17.127371+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAF7 as ready","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:32:17.117036+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: traf7 has been classified as Green List (High Evidence).","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:31:30.735042+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7857","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRAF7 as ready","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:31:30.724519+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7857","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: traf7 has been classified as Green List (High Evidence).","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:31:11.679194+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7857","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRAF7 were changed from  to Cardiac, facial, and digital anomalies with developmental delay, MIM# 618164","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:30:51.248687+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7856","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAF7 were set to ","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:30:18.124348+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7855","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRAF7 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:29:58.634131+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7854","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRAF7: Rating: GREEN; Mode of pathogenicity: None; Publications: 32376980; Phenotypes: Cardiac, facial, and digital anomalies with developmental delay, MIM# 618164; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:29:56.607204+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRAF7 were changed from  to Cardiac, facial, and digital anomalies with developmental delay, MIM# 618164","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:29:01.232229+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAF7 were set to 32376980","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:28:56.184444+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBE3B as ready","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:28:56.175055+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ube3b has been classified as Green List (High Evidence).","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:28:46.042382+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRAF7 were set to ","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:28:16.683049+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRAF7 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:27:46.551088+10:00","panel_name":"Blepharophimosis","panel_id":55,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRAF7: Rating: GREEN; Mode of pathogenicity: None; Publications: 32376980; Phenotypes: Cardiac, facial, and digital anomalies with developmental delay, MIM# 618164; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TRAF7","entity_type":"gene"},{"created":"2021-06-05T17:24:24.434263+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.22","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBE3B as ready","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:24:24.424407+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.22","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ube3b has been classified as Green List (High Evidence).","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:24:19.270934+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.22","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: UBE3B as Green List (high evidence)","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:24:19.260998+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.22","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ube3b has been classified as Green List (High Evidence).","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:23:54.485757+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.197","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBE3B were changed from Kaufman oculocerebrofacial syndrome, MIM# 244450; MONDO:0009485 to Kaufman oculocerebrofacial syndrome, MIM# 244450; MONDO:0009485","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:23:39.864060+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"1.21","user_name":"Zornitza Stark","item_type":"entity","text":"gene: UBE3B was added\ngene: UBE3B was added to Microcephaly. Sources: Expert Review\nMode of inheritance for gene: UBE3B was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: UBE3B were set to 23200864; 23200864; 34012380; 32949109\nPhenotypes for gene: UBE3B were set to Kaufman oculocerebrofacial syndrome, MIM# 244450; MONDO:0009485\nReview for gene: UBE3B was set to GREEN\nAdded comment: Intellectual disability, microcephaly, dysmorphic features, including blepharophimosis and ptosis. Over 20 families reported. \nSources: Expert Review","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:23:26.497293+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.196","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBE3B were changed from  to Kaufman oculocerebrofacial syndrome, MIM# 244450; MONDO:0009485","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:22:08.541505+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.195","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBE3B were set to ","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:21:37.951060+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.194","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: UBE3B: Rating: GREEN; Mode of pathogenicity: None; Publications: 23200864, 23200864, 34012380, 32949109; Phenotypes: Kaufman oculocerebrofacial syndrome, MIM# 244450, MONDO:0009485; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:18:14.715627+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7854","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBE3B as ready","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:18:14.700450+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7854","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ube3b has been classified as Green List (High Evidence).","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:17:06.860059+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7854","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBE3B were changed from  to Kaufman oculocerebrofacial syndrome, MIM# 244450; MONDO:0009485","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:16:43.889681+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7853","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBE3B were set to ","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:14:48.193049+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7852","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UBE3B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:14:30.046778+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7851","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: UBE3B: Rating: GREEN; Mode of pathogenicity: None; Publications: 23200864, 23200864, 34012380, 32949109; Phenotypes: Kaufman oculocerebrofacial syndrome, MIM# 244450, MONDO:0009485; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:13:55.419765+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3809","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBE3B as ready","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:13:55.409592+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3809","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ube3b has been classified as Green List (High Evidence).","entity_name":"UBE3B","entity_type":"gene"},{"created":"2021-06-05T17:13:52.096974+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3809","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBE3B were changed from  to Kaufman oculocerebrofacial syndrome, MIM# 244450; MONDO:0009485","entity_name":"UBE3B","entity_type":"gene"}]}