{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1888","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1886","results":[{"created":"2020-04-02T11:01:05.182461+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1893","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: frmd4a has been classified as Amber List (Moderate Evidence).","entity_name":"FRMD4A","entity_type":"gene"},{"created":"2020-04-02T11:00:46.625774+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1892","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FRMD4A was added\ngene: FRMD4A was added to Mendeliome. Sources: Expert Review\nMode of inheritance for gene: FRMD4A was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FRMD4A were set to 25388005; 30214071\nPhenotypes for gene: FRMD4A were set to Intellectual disability; microcephaly; Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia, MIM# 616819\nReview for gene: FRMD4A was set to AMBER\nAdded comment: Single Bedouin Israeli family reported with homozygous variant initially. Good segregation data. No functional data. Another family reported as part of a large consanguineous microcephaly cohort, different variant. \nSources: Expert Review","entity_name":"FRMD4A","entity_type":"gene"},{"created":"2020-04-02T10:59:50.795252+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2506","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FRMD4A as ready","entity_name":"FRMD4A","entity_type":"gene"},{"created":"2020-04-02T10:59:50.781886+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2506","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: frmd4a has been classified as Amber List (Moderate Evidence).","entity_name":"FRMD4A","entity_type":"gene"},{"created":"2020-04-02T10:59:16.622545+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2506","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FRMD4A were changed from Intellectual disability; microcephaly to Intellectual disability; microcephaly; Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia, MIM# 616819","entity_name":"FRMD4A","entity_type":"gene"},{"created":"2020-04-02T10:58:40.100661+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2505","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FRMD4A as Amber List (moderate evidence)","entity_name":"FRMD4A","entity_type":"gene"},{"created":"2020-04-02T10:58:40.087323+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2505","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: frmd4a has been classified as Amber List (Moderate Evidence).","entity_name":"FRMD4A","entity_type":"gene"},{"created":"2020-04-02T10:58:06.155087+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2504","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FRMD4A: Changed phenotypes: Intellectual disability, microcephaly, Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia, MIM# 616819","entity_name":"FRMD4A","entity_type":"gene"},{"created":"2020-04-02T10:57:57.032576+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2504","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: FRMD4A: Changed phenotypes: Intellectual disability, microcephaly, Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia 616819","entity_name":"FRMD4A","entity_type":"gene"},{"created":"2020-04-02T10:57:17.970358+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2504","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FRMD4A was added\ngene: FRMD4A was added to Intellectual disability syndromic and non-syndromic. Sources: Expert Review\nMode of inheritance for gene: FRMD4A was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FRMD4A were set to 25388005; 30214071\nPhenotypes for gene: FRMD4A were set to Intellectual disability; microcephaly\nReview for gene: FRMD4A was set to AMBER\nAdded comment: Single Bedouin Israeli family reported with homozygous variant initially. Good segregation data. No functional data. Another family reported as part of a large consanguineous microcephaly cohort, different variant. \nSources: Expert Review","entity_name":"FRMD4A","entity_type":"gene"},{"created":"2020-04-02T10:31:15.931170+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"panel","text":"Panel status changed from deleted to public","entity_name":null,"entity_type":null},{"created":"2020-04-02T10:30:24.620777+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Source Expert Review Red was added to NMNAT2.\nSource Research was added to NMNAT2.\nAdded phenotypes polyneuropathy; erythromelalgia for gene: NMNAT2\nRating Changed from Green List (high evidence) to Red List (low evidence)","entity_name":"NMNAT2","entity_type":"gene"},{"created":"2020-04-02T10:30:24.551342+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Source Literature was added to FAAHP1.\nAdded phenotypes Pain insensitivity for gene: FAAHP1","entity_name":"FAAHP1","entity_type":"gene"},{"created":"2020-04-02T10:30:24.494220+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Source Review was added to CLTCL1.\nSource Literaure was added to CLTCL1.\nAdded phenotypes Congenital insensitivity to pain for gene: CLTCL1","entity_name":"CLTCL1","entity_type":"gene"},{"created":"2020-04-02T10:30:24.431288+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Source Expert Review Red was added to CCT5.\nAdded phenotypes Neuropathy, hereditary sensory, with spastic paraplegia, 256840; HSAN with spastic paraplegia for gene: CCT5\nRating Changed from Green List (high evidence) to Red List (low evidence)","entity_name":"CCT5","entity_type":"gene"},{"created":"2020-04-02T10:30:24.369610+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Source Expert Review Amber was added to NAGLU.\nAdded phenotypes Late-onset painful sensory neuropathy, AD; Mucopolysaccharidosis type IIIB (Sanfilippo B), AR, 252920 for gene: NAGLU\nRating Changed from Green List (high evidence) to Amber List (moderate evidence)","entity_name":"NAGLU","entity_type":"gene"},{"created":"2020-04-02T10:30:24.309583+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Source Expert Review Amber was added to MPV17.\nAdded phenotypes Navajo neurohepatopathy; Mitochondrial DNA depletion syndrome 6 (hepatocerebral type), 256810; Pain insensitivity for gene: MPV17\nRating Changed from Green List (high evidence) to Amber List (moderate evidence)","entity_name":"MPV17","entity_type":"gene"},{"created":"2020-04-02T10:30:24.249435+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Neuropathy, hereditary sensory and autonomic, type II, 201300; HSAN 2; Hereditary sensory and autonomic neuropathy type IIA for gene: WNK1","entity_name":"WNK1","entity_type":"gene"},{"created":"2020-04-02T10:30:24.197183+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hereditary amyloidosis; Amyloidosis, hereditary, transthyretin-related, 105210; Familial amyloid polyneuropathy; Carpal tunnel syndrome, familial, 115430 for gene: TTR","entity_name":"TTR","entity_type":"gene"},{"created":"2020-04-02T10:30:24.145268+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Familial episodic pain syndrome type I; Episodic pain syndrome, familial,  615040 for gene: TRPA1","entity_name":"TRPA1","entity_type":"gene"},{"created":"2020-04-02T10:30:24.092967+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hereditary sensory and autonomic neuropathy type IC; HSAN 1; Neuropathy, hereditary sensory and autonomic, type IC, 613640 for gene: SPTLC2","entity_name":"SPTLC2","entity_type":"gene"},{"created":"2020-04-02T10:30:24.040404+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Neuropathy, hereditary sensory and autonomic, type IA, 162400; HSAN 1; Hereditary sensory neuropathy type IA for gene: SPTLC1","entity_name":"SPTLC1","entity_type":"gene"},{"created":"2020-04-02T10:30:23.980500+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Amyotrophy, hereditary neuralgic, 162100; Hereditary neuralgic amyotrophy for gene: SEPT9","entity_name":"SEPT9","entity_type":"gene"},{"created":"2020-04-02T10:30:23.926202+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes HSAN2D, autosomal recessive, AR, 243000; Erythermalgia, primary, AD, 133020; Insensitivity to pain, congenital, AR, 243000; Small fiber neuropathy, AD,133020; Paroxysmal extreme pain disorder, AD, 167400 for gene: SCN9A","entity_name":"SCN9A","entity_type":"gene"},{"created":"2020-04-02T10:30:23.873817+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Neuropathy, hereditary sensory and autonomic, type VII, 615548; Episodic pain syndrome, familial, 3, 615552; Hereditary sensory and autonomic neuropathy type VII; Familial episodic pain syndrome for gene: SCN11A","entity_name":"SCN11A","entity_type":"gene"},{"created":"2020-04-02T10:30:23.820730+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Small fibre neuropathy; Painful small fibre neuropathy; SFN; Episodic pain syndrome, familial, 2, 615551; Familial episodic pain syndrome-2 for gene: SCN10A","entity_name":"SCN10A","entity_type":"gene"},{"created":"2020-04-02T10:30:23.764149+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hereditary sensory and autonomic neuropathy; Neuropathy, hereditary sensory and autonomic, type IIB, 613115; HSAN 2B for gene: RETREG1","entity_name":"RETREG1","entity_type":"gene"},{"created":"2020-04-02T10:30:23.711680+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes HSAN1/2B; Hereditary motor and sensory neuropathy IIB; Charcot-Marie-Tooth disease, type 2B, 600882 for gene: RAB7A","entity_name":"RAB7A","entity_type":"gene"},{"created":"2020-04-02T10:30:23.655815+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Cerebral amyloid angiopathy, PRNP-related,\t137440 for gene: PRNP","entity_name":"PRNP","entity_type":"gene"},{"created":"2020-04-02T10:30:23.603963+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes insensitivity to pain; Neuropathy, hereditary sensory and autonomic, type VIII, 616488; HSAN VIII; HSAN 8; Hereditary sensory and autonomic neuropathy type VIII for gene: PRDM12","entity_name":"PRDM12","entity_type":"gene"},{"created":"2020-04-02T10:30:23.550602+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes HSAN 4; Insensitivity to pain, congenital, with anhidrosis, 256800; Hereditary sensory neuropathy type IV for gene: NTRK1","entity_name":"NTRK1","entity_type":"gene"},{"created":"2020-04-02T10:30:23.498470+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Neuropathy, hereditary sensory and autonomic, type V, 608654; HSAN 5; Congenital sensory neuropathy with selective loss of small myelinated fibers; Hereditary sensory neuropathy type V for gene: NGF","entity_name":"NGF","entity_type":"gene"},{"created":"2020-04-02T10:30:23.444804+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Hereditary Sensory and Autonomic Neuropathy, Type II; Neuropathy, hereditary sensory, type IIC, 614213 for gene: KIF1A","entity_name":"KIF1A","entity_type":"gene"},{"created":"2020-04-02T10:30:23.390676+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Fabry disease,\t301500 for gene: GLA","entity_name":"GLA","entity_type":"gene"},{"created":"2020-04-02T10:30:23.336452+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Familial dysautonomia; NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; Dysautonomia, familial, 223900 for gene: ELP1","entity_name":"ELP1","entity_type":"gene"},{"created":"2020-04-02T10:30:23.284184+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes Neuropathy, hereditary sensory, type IF, 615632; HSN1F for gene: ATL3","entity_name":"ATL3","entity_type":"gene"},{"created":"2020-04-02T10:30:23.228605+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Added phenotypes HSN1D; Neuropathy, hereditary sensory, type ID, 613708; Hereditary spastic paraplegia, 182600; Hereditary sensory neuropathy for gene: ATL1","entity_name":"ATL1","entity_type":"gene"},{"created":"2020-04-02T10:26:38.056321+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"panel","text":"Panel status changed from public to deleted","entity_name":null,"entity_type":null},{"created":"2020-04-02T10:25:04.861375+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"panel","text":"Panel status changed from internal to public\nPanel types changed to Victorian Clinical Genetics Services; Rare Disease","entity_name":null,"entity_type":null},{"created":"2020-04-02T10:22:05.418696+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NMNAT2 was added\ngene: NMNAT2 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: NMNAT2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NMNAT2 were set to 31132363\nPhenotypes for gene: NMNAT2 were set to polyneuropathy; erythromelalgia","entity_name":"NMNAT2","entity_type":"gene"},{"created":"2020-04-02T10:22:05.370688+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: FAAHP1 was added\ngene: FAAHP1 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: FAAHP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FAAHP1 were set to 30929760\nPhenotypes for gene: FAAHP1 were set to Pain insensitivity","entity_name":"FAAHP1","entity_type":"gene"},{"created":"2020-04-02T10:22:05.324196+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CLTCL1 was added\ngene: CLTCL1 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: CLTCL1 was set to Unknown\nPublications for gene: CLTCL1 were set to 26068709\nPhenotypes for gene: CLTCL1 were set to Congenital insensitivity to pain","entity_name":"CLTCL1","entity_type":"gene"},{"created":"2020-04-02T10:22:05.276874+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CCT5 was added\ngene: CCT5 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: CCT5 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CCT5 were set to 12874111; 16399879; 25124038; 28623285\nPhenotypes for gene: CCT5 were set to Neuropathy, hereditary sensory, with spastic paraplegia, 256840; HSAN with spastic paraplegia","entity_name":"CCT5","entity_type":"gene"},{"created":"2020-04-02T10:22:05.230023+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NAGLU was added\ngene: NAGLU was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: NAGLU was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: NAGLU were set to 25818867; 12202988\nPhenotypes for gene: NAGLU were set to Late-onset painful sensory neuropathy, AD; Mucopolysaccharidosis type IIIB (Sanfilippo B), AR, 252920","entity_name":"NAGLU","entity_type":"gene"},{"created":"2020-04-02T10:22:05.179880+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MPV17 was added\ngene: MPV17 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: MPV17 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: MPV17 were set to 16582910; 16909392; 23714749; 22508010; 185990; 11431741\nPhenotypes for gene: MPV17 were set to Navajo neurohepatopathy; Mitochondrial DNA depletion syndrome 6 (hepatocerebral type), 256810; Pain insensitivity","entity_name":"MPV17","entity_type":"gene"},{"created":"2020-04-02T10:22:05.134225+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: WNK1 was added\ngene: WNK1 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: WNK1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: WNK1 were set to 15911806; 16636245; 16946995; 21625937; 15455397; 18521183; 15060842\nPhenotypes for gene: WNK1 were set to Neuropathy, hereditary sensory and autonomic, type II, 201300; HSAN 2; Hereditary sensory and autonomic neuropathy type IIA","entity_name":"WNK1","entity_type":"gene"},{"created":"2020-04-02T10:22:05.088014+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TTR was added\ngene: TTR was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: TTR was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: TTR were set to 14640030; 26800456; 12771253; 30120737; 16433699; 25069833; 30878017; 31111153; 31118583; 28678039; 19365058; 31131842; 8309582; The Metabolic and Molecular Bases of Inherited Disease. Vol. IV. 8th ed.Benson, M. D. Amyloidosis. In: Scriver, C. R et al.: New York: McGraw-Hill . 2001; 3011930\nPhenotypes for gene: TTR were set to Hereditary amyloidosis; Amyloidosis, hereditary, transthyretin-related, 105210; Familial amyloid polyneuropathy; Carpal tunnel syndrome, familial, 115430","entity_name":"TTR","entity_type":"gene"},{"created":"2020-04-02T10:22:05.040854+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TRPA1 was added\ngene: TRPA1 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: TRPA1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: TRPA1 were set to 28314413; 21468319; 24778270; 20718100; 16564016; 28436534; 24564660; 20547126\nPhenotypes for gene: TRPA1 were set to Familial episodic pain syndrome type I; Episodic pain syndrome, familial,  615040","entity_name":"TRPA1","entity_type":"gene"},{"created":"2020-04-02T10:22:04.994225+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SPTLC2 was added\ngene: SPTLC2 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: SPTLC2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: SPTLC2 were set to 26681808; 23658386; 12207934; 27025386; 20920666\nPhenotypes for gene: SPTLC2 were set to Hereditary sensory and autonomic neuropathy type IC; HSAN 1; Neuropathy, hereditary sensory and autonomic, type IC, 613640","entity_name":"SPTLC2","entity_type":"gene"},{"created":"2020-04-02T10:22:04.941596+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SPTLC1 was added\ngene: SPTLC1 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: SPTLC1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: SPTLC1 were set to 11242114; 11242106; 15037712\nPhenotypes for gene: SPTLC1 were set to Neuropathy, hereditary sensory and autonomic, type IA, 162400; HSAN 1; Hereditary sensory neuropathy type IA","entity_name":"SPTLC1","entity_type":"gene"},{"created":"2020-04-02T10:22:04.895919+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SEPT9 was added\ngene: SEPT9 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: SEPT9 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: SEPT9 were set to 21556032; 16186812; 19451530\nPhenotypes for gene: SEPT9 were set to Amyotrophy, hereditary neuralgic, 162100; Hereditary neuralgic amyotrophy","entity_name":"SEPT9","entity_type":"gene"},{"created":"2020-04-02T10:22:04.846308+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SCN9A was added\ngene: SCN9A was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: SCN9A was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: SCN9A were set to 16392115; 17167479; 17470132; 17145499; 17679678; 25316021; 15958509; 28665811; 23596073; 24817410; 28235406; 16216943; 24813307; 14985375; 1536168\nPhenotypes for gene: SCN9A were set to HSAN2D, autosomal recessive, AR, 243000; Erythermalgia, primary, AD, 133020; Insensitivity to pain, congenital, AR, 243000; Small fiber neuropathy, AD,133020; Paroxysmal extreme pain disorder, AD, 167400","entity_name":"SCN9A","entity_type":"gene"},{"created":"2020-04-02T10:22:04.801193+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SCN11A was added\ngene: SCN11A was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: SCN11A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: SCN11A were set to 28298626; 24776970; 25316021; 24207120; 27503742; 24036948; 28665811; 24813307; 26645915\nPhenotypes for gene: SCN11A were set to Neuropathy, hereditary sensory and autonomic, type VII, 615548; Episodic pain syndrome, familial, 3, 615552; Hereditary sensory and autonomic neuropathy type VII; Familial episodic pain syndrome","entity_name":"SCN11A","entity_type":"gene"},{"created":"2020-04-02T10:22:04.755449+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SCN10A was added\ngene: SCN10A was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: SCN10A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: SCN10A were set to 23115331; 26711856; 24776970; 25316021; 25250524; 24006052; 28665811; 27598514; 24813307\nPhenotypes for gene: SCN10A were set to Small fibre neuropathy; Painful small fibre neuropathy; SFN; Episodic pain syndrome, familial, 2, 615551; Familial episodic pain syndrome-2","entity_name":"SCN10A","entity_type":"gene"},{"created":"2020-04-02T10:22:04.710248+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RETREG1 was added\ngene: RETREG1 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: RETREG1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: RETREG1 were set to 19838196; 21115472; 24327336\nPhenotypes for gene: RETREG1 were set to Hereditary sensory and autonomic neuropathy; Neuropathy, hereditary sensory and autonomic, type IIB, 613115; HSAN 2B","entity_name":"RETREG1","entity_type":"gene"},{"created":"2020-04-02T10:22:04.665931+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: RAB7A was added\ngene: RAB7A was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: RAB7A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: RAB7A were set to 17060578; 15455439; 12545426\nPhenotypes for gene: RAB7A were set to HSAN1/2B; Hereditary motor and sensory neuropathy IIB; Charcot-Marie-Tooth disease, type 2B, 600882","entity_name":"RAB7A","entity_type":"gene"},{"created":"2020-04-02T10:22:04.621755+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PRNP was added\ngene: PRNP was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: PRNP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PRNP were set to 27716661; 24224623; 25287017; 26768678\nPhenotypes for gene: PRNP were set to Cerebral amyloid angiopathy, PRNP-related,\t137440","entity_name":"PRNP","entity_type":"gene"},{"created":"2020-04-02T10:22:04.577662+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PRDM12 was added\ngene: PRDM12 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: PRDM12 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PRDM12 were set to 26975306; 25891934; 26005867\nPhenotypes for gene: PRDM12 were set to insensitivity to pain; Neuropathy, hereditary sensory and autonomic, type VIII, 616488; HSAN VIII; HSAN 8; Hereditary sensory and autonomic neuropathy type VIII","entity_name":"PRDM12","entity_type":"gene"},{"created":"2020-04-02T10:22:04.533592+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NTRK1 was added\ngene: NTRK1 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: NTRK1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NTRK1 were set to 11668614; 8696348; 18077166\nPhenotypes for gene: NTRK1 were set to HSAN 4; Insensitivity to pain, congenital, with anhidrosis, 256800; Hereditary sensory neuropathy type IV","entity_name":"NTRK1","entity_type":"gene"},{"created":"2020-04-02T10:22:04.489282+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NGF was added\ngene: NGF was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: NGF was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NGF were set to 26562335; 20978020; 14976160; 15131306\nPhenotypes for gene: NGF were set to Neuropathy, hereditary sensory and autonomic, type V, 608654; HSAN 5; Congenital sensory neuropathy with selective loss of small myelinated fibers; Hereditary sensory neuropathy type V","entity_name":"NGF","entity_type":"gene"},{"created":"2020-04-02T10:22:04.445134+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KIF1A was added\ngene: KIF1A was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: KIF1A was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: KIF1A were set to 25265257; 21820098\nPhenotypes for gene: KIF1A were set to Hereditary Sensory and Autonomic Neuropathy, Type II; Neuropathy, hereditary sensory, type IIC, 614213","entity_name":"KIF1A","entity_type":"gene"},{"created":"2020-04-02T10:22:04.400150+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GLA was added\ngene: GLA was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: GLA was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)\nPhenotypes for gene: GLA were set to Fabry disease,\t301500","entity_name":"GLA","entity_type":"gene"},{"created":"2020-04-02T10:22:04.356399+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ELP1 was added\ngene: ELP1 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: ELP1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ELP1 were set to 17985250; 11179021; 11179008; 8102296\nPhenotypes for gene: ELP1 were set to Familial dysautonomia; NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; Dysautonomia, familial, 223900","entity_name":"ELP1","entity_type":"gene"},{"created":"2020-04-02T10:22:04.312832+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ATL3 was added\ngene: ATL3 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: ATL3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: ATL3 were set to 24459106; 24736309\nPhenotypes for gene: ATL3 were set to Neuropathy, hereditary sensory, type IF, 615632; HSN1F","entity_name":"ATL3","entity_type":"gene"},{"created":"2020-04-02T10:22:04.265822+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ATL1 was added\ngene: ATL1 was added to Pain syndromes. Sources: Genomics England PanelApp,Expert Review Green\nMode of inheritance for gene: ATL1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: ATL1 were set to 21194679; 22340599\nPhenotypes for gene: ATL1 were set to HSN1D; Neuropathy, hereditary sensory, type ID, 613708; Hereditary spastic paraplegia, 182600; Hereditary sensory neuropathy","entity_name":"ATL1","entity_type":"gene"},{"created":"2020-04-02T10:22:04.237104+11:00","panel_name":"Pain syndromes","panel_id":3126,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Pain syndromes","entity_name":null,"entity_type":null},{"created":"2020-04-01T21:18:13.588008+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.4","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: UNC45A as Amber List (moderate evidence)","entity_name":"UNC45A","entity_type":"gene"},{"created":"2020-04-01T21:18:13.581883+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.4","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on list classification: Not enough evidence currently to determine bone fragility is a prominent feature of the condition.","entity_name":"UNC45A","entity_type":"gene"},{"created":"2020-04-01T21:18:13.547367+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.4","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: unc45a has been classified as Amber List (Moderate Evidence).","entity_name":"UNC45A","entity_type":"gene"},{"created":"2020-04-01T21:16:55.355197+11:00","panel_name":"Osteogenesis Imperfecta","panel_id":147,"panel_version":"0.3","user_name":"Bryony Thompson","item_type":"entity","text":"reviewed gene: UNC45A: Rating: AMBER; Mode of pathogenicity: None; Publications: 29429573; Phenotypes: cholestasis, congenital diarrhea, impaired hearing, bone fragility; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"UNC45A","entity_type":"gene"},{"created":"2020-04-01T21:10:59.065264+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1891","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEK10 as ready","entity_name":"NEK10","entity_type":"gene"},{"created":"2020-04-01T21:10:59.052450+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1891","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nek10 has been classified as Green List (High Evidence).","entity_name":"NEK10","entity_type":"gene"},{"created":"2020-04-01T21:10:49.180934+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1891","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NEK10 as Green List (high evidence)","entity_name":"NEK10","entity_type":"gene"},{"created":"2020-04-01T21:10:49.167191+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1891","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nek10 has been classified as Green List (High Evidence).","entity_name":"NEK10","entity_type":"gene"},{"created":"2020-04-01T21:10:34.838264+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NEK10 as ready","entity_name":"NEK10","entity_type":"gene"},{"created":"2020-04-01T21:10:34.824910+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nek10 has been classified as Green List (High Evidence).","entity_name":"NEK10","entity_type":"gene"},{"created":"2020-04-01T21:04:49.238451+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1890","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NEK10 was added\ngene: NEK10 was added to Mendeliome. Sources: NHS GMS\nMode of inheritance for gene: NEK10 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NEK10 were set to 31959991\nPhenotypes for gene: NEK10 were set to Primary ciliary dyskinesia; bronchiectasis\nReview for gene: NEK10 was set to GREEN\nAdded comment: Nine individuals from 5 unrelated families, some functional data. \nSources: NHS GMS","entity_name":"NEK10","entity_type":"gene"},{"created":"2020-04-01T21:03:48.597421+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NEK10 were changed from  to Primary ciliary dyskinesia; bronchiectasis","entity_name":"NEK10","entity_type":"gene"},{"created":"2020-04-01T21:03:26.799369+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NEK10 as Green List (high evidence)","entity_name":"NEK10","entity_type":"gene"},{"created":"2020-04-01T21:03:26.782234+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nek10 has been classified as Green List (High Evidence).","entity_name":"NEK10","entity_type":"gene"},{"created":"2020-04-01T21:02:18.122930+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NEK10 was added\ngene: NEK10 was added to Ciliary Dyskinesia. Sources: NHS GMS\nMode of inheritance for gene: NEK10 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: NEK10 were set to 31959991\nReview for gene: NEK10 was set to GREEN\ngene: NEK10 was marked as current diagnostic\nAdded comment: Nine individuals from 5 unrelated families, some functional data. \nSources: NHS GMS","entity_name":"NEK10","entity_type":"gene"},{"created":"2020-04-01T20:51:01.954450+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.644","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIGK as ready","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:51:01.939122+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.644","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pigk has been classified as Green List (High Evidence).","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:50:57.520675+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.644","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PIGK as Green List (high evidence)","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:50:57.512309+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.644","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pigk has been classified as Green List (High Evidence).","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:50:28.700222+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.643","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PIGK was added\ngene: PIGK was added to Genetic Epilepsy. Sources: Literature\nMode of inheritance for gene: PIGK was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PIGK were set to 32220290\nPhenotypes for gene: PIGK were set to Intellectual disability; seizures; cerebellar atrophy\nReview for gene: PIGK was set to GREEN\nAdded comment: 12 individuals from 9 unrelated families reported. \nSources: Literature","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:49:01.184586+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1889","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIGK as ready","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:49:01.174574+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1889","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pigk has been classified as Green List (High Evidence).","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:48:52.170127+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1889","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PIGK as Green List (high evidence)","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:48:52.157220+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1889","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pigk has been classified as Green List (High Evidence).","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:48:12.647573+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1888","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PIGK was added\ngene: PIGK was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: PIGK was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PIGK were set to 32220290\nPhenotypes for gene: PIGK were set to Intellectual disability; seizures; cerebellar atrophy\nReview for gene: PIGK was set to GREEN\nAdded comment: 12 individuals from 9 unrelated families reported. \nSources: Literature","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:47:15.368084+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2503","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PIGK as Green List (high evidence)","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:47:15.354429+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pigk has been classified as Green List (High Evidence).","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:46:17.433707+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2502","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PIGK was added\ngene: PIGK was added to Intellectual disability syndromic and non-syndromic. Sources: Literature\nMode of inheritance for gene: PIGK was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PIGK were set to 32220290\nPhenotypes for gene: PIGK were set to Intellectual disability; seizures; cerebellar atrophy\nReview for gene: PIGK was set to GREEN\nAdded comment: 12 individuals from 9 unrelated families reported. \nSources: Literature","entity_name":"PIGK","entity_type":"gene"},{"created":"2020-04-01T20:43:06.510862+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ADARB1 as Green List (high evidence)","entity_name":"ADARB1","entity_type":"gene"},{"created":"2020-04-01T20:43:06.502148+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adarb1 has been classified as Green List (High Evidence).","entity_name":"ADARB1","entity_type":"gene"},{"created":"2020-04-01T20:42:38.669867+11:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ADARB1 was added\ngene: ADARB1 was added to Microcephaly. Sources: Literature\nMode of inheritance for gene: ADARB1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ADARB1 were set to 32220291\nPhenotypes for gene: ADARB1 were set to Intellectual disability; microcephaly; seizures\nReview for gene: ADARB1 was set to GREEN\nAdded comment: Four unrelated individuals with bi-allelic variants in this gene. \nSources: Literature","entity_name":"ADARB1","entity_type":"gene"},{"created":"2020-04-01T20:39:38.738177+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.642","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ADARB1 as Green List (high evidence)","entity_name":"ADARB1","entity_type":"gene"},{"created":"2020-04-01T20:39:38.729596+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.642","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adarb1 has been classified as Green List (High Evidence).","entity_name":"ADARB1","entity_type":"gene"},{"created":"2020-04-01T20:39:07.638963+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.641","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ADARB1 was added\ngene: ADARB1 was added to Genetic Epilepsy. Sources: Literature\nMode of inheritance for gene: ADARB1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ADARB1 were set to 32220291\nPhenotypes for gene: ADARB1 were set to Intellectual disability; microcephaly; seizures\nReview for gene: ADARB1 was set to GREEN\nAdded comment: Four unrelated individuals with bi-allelic variants in this gene. \nSources: Literature","entity_name":"ADARB1","entity_type":"gene"}]}