{"count":220314,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1451","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1449","results":[{"created":"2021-01-05T20:37:09.515806+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC10A2 were changed from  to Bile acid malabsorption, primary, MIM# 613291","entity_name":"SLC10A2","entity_type":"gene"},{"created":"2021-01-05T20:36:45.908195+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC10A2 were set to ","entity_name":"SLC10A2","entity_type":"gene"},{"created":"2021-01-05T20:36:23.047503+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC10A2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC10A2","entity_type":"gene"},{"created":"2021-01-05T20:35:54.435027+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC10A2 as Red List (low evidence)","entity_name":"SLC10A2","entity_type":"gene"},{"created":"2021-01-05T20:35:54.425142+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc10a2 has been classified as Red List (Low Evidence).","entity_name":"SLC10A2","entity_type":"gene"},{"created":"2021-01-05T20:35:26.412862+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC10A2: Rating: RED; Mode of pathogenicity: None; Publications: 9109432; Phenotypes: Bile acid malabsorption, primary, MIM# 613291; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC10A2","entity_type":"gene"},{"created":"2021-01-05T20:30:31.394009+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SKIV2L as ready","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2021-01-05T20:30:31.383581+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: skiv2l has been classified as Green List (High Evidence).","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2021-01-05T20:28:23.006085+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SKIV2L were changed from  to Trichohepatoenteric syndrome 2, MIM# 614602","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2021-01-05T20:27:55.753778+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SKIV2L were set to ","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2021-01-05T20:27:24.981754+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SKIV2L was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2021-01-05T20:26:57.753604+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SKIV2L: Rating: GREEN; Mode of pathogenicity: None; Publications: 22444670, 33114497, 30397475, 29527791, 29484573; Phenotypes: Trichohepatoenteric syndrome 2, MIM# 614602; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SKIV2L","entity_type":"gene"},{"created":"2021-01-05T20:23:58.475359+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5942","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLVAP as ready","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T20:23:58.464010+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5942","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plvap has been classified as Green List (High Evidence).","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T20:23:50.359263+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SI as ready","entity_name":"SI","entity_type":"gene"},{"created":"2021-01-05T20:23:50.348769+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: si has been classified as Green List (High Evidence).","entity_name":"SI","entity_type":"gene"},{"created":"2021-01-05T20:23:47.301527+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SI were set to ","entity_name":"SI","entity_type":"gene"},{"created":"2021-01-05T20:23:17.202850+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SI were changed from  to Sucrase-isomaltase deficiency, congenital, MIM# 222900","entity_name":"SI","entity_type":"gene"},{"created":"2021-01-05T20:22:49.816444+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SI was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SI","entity_type":"gene"},{"created":"2021-01-05T20:22:19.329994+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SI: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Sucrase-isomaltase deficiency, congenital, MIM# 222900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SI","entity_type":"gene"},{"created":"2021-01-05T20:21:27.927752+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SBDS as ready","entity_name":"SBDS","entity_type":"gene"},{"created":"2021-01-05T20:21:27.913465+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sbds has been classified as Green List (High Evidence).","entity_name":"SBDS","entity_type":"gene"},{"created":"2021-01-05T20:18:34.603133+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SBDS were changed from  to Shwachman-Diamond syndrome, MIM# 260400","entity_name":"SBDS","entity_type":"gene"},{"created":"2021-01-05T20:16:25.200617+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SBDS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SBDS","entity_type":"gene"},{"created":"2021-01-05T20:15:56.792723+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SBDS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Shwachman-Diamond syndrome, MIM# 260400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SBDS","entity_type":"gene"},{"created":"2021-01-05T19:45:00.357347+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SAR1B as ready","entity_name":"SAR1B","entity_type":"gene"},{"created":"2021-01-05T19:45:00.347156+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sar1b has been classified as Green List (High Evidence).","entity_name":"SAR1B","entity_type":"gene"},{"created":"2021-01-05T19:44:55.278550+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SAR1B were changed from  to Chylomicron retention disease, MIM# 246700","entity_name":"SAR1B","entity_type":"gene"},{"created":"2021-01-05T19:44:24.486406+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SAR1B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SAR1B","entity_type":"gene"},{"created":"2021-01-05T19:43:55.338562+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SAR1B: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Chylomicron retention disease, MIM# 246700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SAR1B","entity_type":"gene"},{"created":"2021-01-05T19:42:08.009528+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRSS1 as ready","entity_name":"PRSS1","entity_type":"gene"},{"created":"2021-01-05T19:42:07.998574+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prss1 has been classified as Green List (High Evidence).","entity_name":"PRSS1","entity_type":"gene"},{"created":"2021-01-05T19:41:58.412422+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRSS1 were changed from  to Pancreatitis, hereditary, MIM# 167800","entity_name":"PRSS1","entity_type":"gene"},{"created":"2021-01-05T19:41:30.455872+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRSS1 were set to ","entity_name":"PRSS1","entity_type":"gene"},{"created":"2021-01-05T19:40:38.682048+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRSS1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRSS1","entity_type":"gene"},{"created":"2021-01-05T19:40:08.035737+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRSS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22379635; Phenotypes: Pancreatitis, hereditary, MIM# 167800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRSS1","entity_type":"gene"},{"created":"2021-01-05T19:35:32.943249+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5942","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PLVAP were changed from  to Diarrhoea 10, protein-losing enteropathy type, MIM# 618183","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T19:35:14.722381+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5941","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PLVAP were set to ","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T19:34:54.305715+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5940","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PLVAP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T19:34:34.685294+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5939","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PLVAP: Rating: GREEN; Mode of pathogenicity: None; Publications: 29875123, 29661969, 26207260, 31215290; Phenotypes: Diarrhoea 10, protein-losing enteropathy type, MIM# 618183; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T19:34:23.288887+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLVAP as ready","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T19:34:23.280238+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plvap has been classified as Green List (High Evidence).","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T19:33:53.538850+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PLVAP were changed from  to Diarrhoea 10, protein-losing enteropathy type, MIM# 618183","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T19:33:22.457942+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PLVAP were set to ","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T19:32:54.521313+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PLVAP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T19:32:25.914792+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PLVAP: Rating: GREEN; Mode of pathogenicity: None; Publications: 29875123, 29661969, 26207260, 31215290; Phenotypes: Diarrhea 10, protein-losing enteropathy type, MIM# 618183; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PLVAP","entity_type":"gene"},{"created":"2021-01-05T16:30:48.173072+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCSK1 as ready","entity_name":"PCSK1","entity_type":"gene"},{"created":"2021-01-05T16:30:48.162705+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcsk1 has been classified as Green List (High Evidence).","entity_name":"PCSK1","entity_type":"gene"},{"created":"2021-01-05T13:16:13.325001+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCSK1 were changed from  to Obesity with impaired prohormone processing, MIM# 600955","entity_name":"PCSK1","entity_type":"gene"},{"created":"2021-01-05T13:15:45.050565+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PCSK1 were set to ","entity_name":"PCSK1","entity_type":"gene"},{"created":"2021-01-05T13:15:14.342579+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PCSK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PCSK1","entity_type":"gene"},{"created":"2021-01-05T13:14:46.315981+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PCSK1: Rating: GREEN; Mode of pathogenicity: None; Publications: 14617756, 17595246; Phenotypes: Obesity with impaired prohormone processing, MIM# 600955; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PCSK1","entity_type":"gene"},{"created":"2021-01-05T13:06:42.840131+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.193","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEUROG3 as ready","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T13:06:42.831789+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.193","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: neurog3 has been classified as Green List (High Evidence).","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T13:05:45.492592+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.193","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NEUROG3 were changed from Diarrhea 4, malabsorptive, congenital to Diarrhoea 4, malabsorptive, congenital, MIM# 610370","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T13:05:34.183307+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.192","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NEUROG3 were set to ","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:59:28.418771+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.191","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NEUROG3 as Green List (high evidence)","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:59:28.406827+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.191","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: neurog3 has been classified as Green List (High Evidence).","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:59:15.852182+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.190","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NEUROG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 16855267, 32574610, 28724572, 21490072; Phenotypes: Diarrhoea 4, malabsorptive, congenital, MIM# 610370; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:56:26.707180+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5939","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEUROG3 as ready","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:56:26.684034+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5939","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: neurog3 has been classified as Green List (High Evidence).","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:56:17.729143+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5939","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NEUROG3 were changed from  to Diarrhoea 4, malabsorptive, congenital, MIM# 610370","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:55:51.191914+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5938","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NEUROG3 were set to ","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:55:15.921750+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5937","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NEUROG3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:53:56.383652+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5936","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NEUROG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 16855267, 32574610, 28724572, 21490072; Phenotypes: Diarrhoea 4, malabsorptive, congenital, MIM# 610370; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:51:42.171407+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEUROG3 as ready","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:51:42.162377+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: neurog3 has been classified as Green List (High Evidence).","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:51:23.933622+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NEUROG3 were changed from  to Diarrhoea 4, malabsorptive, congenital, MIM# 610370","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:51:00.337149+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NEUROG3 were set to ","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:49:12.784830+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NEUROG3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:48:43.602493+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NEUROG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 16855267, 32574610, 28724572, 21490072; Phenotypes: Diarrhea 4, malabsorptive, congenital, MIM# 610370; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NEUROG3","entity_type":"gene"},{"created":"2021-01-05T12:44:39.347822+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GUCY2C as ready","entity_name":"GUCY2C","entity_type":"gene"},{"created":"2021-01-05T12:44:39.339276+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gucy2c has been classified as Green List (High Evidence).","entity_name":"GUCY2C","entity_type":"gene"},{"created":"2021-01-05T12:44:35.719514+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GUCY2C were changed from  to Diarrhoea 6, MIM# 614616","entity_name":"GUCY2C","entity_type":"gene"},{"created":"2021-01-05T12:43:45.706431+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GUCY2C were set to ","entity_name":"GUCY2C","entity_type":"gene"},{"created":"2021-01-05T12:43:17.320981+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: GUCY2C was changed from  to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"GUCY2C","entity_type":"gene"},{"created":"2021-01-05T12:41:42.625074+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GUCY2C was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GUCY2C","entity_type":"gene"},{"created":"2021-01-05T12:41:13.118005+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GUCY2C: Rating: GREEN; Mode of pathogenicity: Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments; Publications: 22521417, 22436048, 25994218, 30353760, 28957388; Phenotypes: Diarrhoea 6, MIM# 614616; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GUCY2C","entity_type":"gene"},{"created":"2021-01-05T11:15:22.407782+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMPRSS15 as ready","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:15:22.398925+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmprss15 has been classified as Green List (High Evidence).","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:15:19.598973+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMPRSS15 were changed from  to Enterokinase deficiency, MIM# 226200","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:14:55.593167+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5936","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMPRSS15 as ready","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:14:55.581997+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5936","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmprss15 has been classified as Green List (High Evidence).","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:14:48.285525+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5936","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMPRSS15 were changed from  to Enterokinase deficiency, MIM# 226200","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:14:29.822627+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5935","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMPRSS15 were set to ","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:14:11.721776+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5934","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMPRSS15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:13:55.539718+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMPRSS15 were set to ","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:13:52.605244+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5933","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TMPRSS15: Rating: GREEN; Mode of pathogenicity: None; Publications: 11719902, 33061943; Phenotypes: Enterokinase deficiency, MIM# 226200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:13:18.687271+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMPRSS15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:10:54.023019+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TMPRSS15: Rating: GREEN; Mode of pathogenicity: None; Publications: 11719902, 33061943; Phenotypes: Enterokinase deficiency, MIM# 226200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMPRSS15","entity_type":"gene"},{"created":"2021-01-05T11:06:20.922160+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5933","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC37 as ready","entity_name":"TTC37","entity_type":"gene"},{"created":"2021-01-05T11:06:20.913735+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5933","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc37 has been classified as Green List (High Evidence).","entity_name":"TTC37","entity_type":"gene"},{"created":"2021-01-05T11:06:09.315883+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5933","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC37 were changed from  to Trichohepatoenteric syndrome 1, MIM# 222470","entity_name":"TTC37","entity_type":"gene"},{"created":"2021-01-05T11:05:51.237757+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5932","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC37 were set to ","entity_name":"TTC37","entity_type":"gene"},{"created":"2021-01-05T11:05:33.198951+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5931","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TTC37 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC37","entity_type":"gene"},{"created":"2021-01-05T11:05:13.106608+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5930","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TTC37: Rating: GREEN; Mode of pathogenicity: None; Publications: 20176027, 17318842; Phenotypes: Trichohepatoenteric syndrome 1, MIM# 222470; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC37","entity_type":"gene"},{"created":"2021-01-05T11:04:54.893155+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC37 as ready","entity_name":"TTC37","entity_type":"gene"},{"created":"2021-01-05T11:04:54.879346+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc37 has been classified as Green List (High Evidence).","entity_name":"TTC37","entity_type":"gene"},{"created":"2021-01-05T11:04:43.447703+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC37 were changed from  to Trichohepatoenteric syndrome 1, MIM# 222470","entity_name":"TTC37","entity_type":"gene"},{"created":"2021-01-05T11:04:15.109022+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC37 were set to ","entity_name":"TTC37","entity_type":"gene"}]}