{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1912","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1910","results":[{"created":"2020-03-04T10:44:01.137985+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1613","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WNT3 were changed from  to Tetra-amelia syndrome 1, MIM# 273395","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:43:40.332051+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1612","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WNT3 were set to ","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:43:20.356031+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1611","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WNT3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:43:03.250802+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1610","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: WNT3 as Red List (low evidence)","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:43:03.237368+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1610","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wnt3 has been classified as Red List (Low Evidence).","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:42:40.400194+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1609","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WNT3: Rating: RED; Mode of pathogenicity: None; Publications: 14872406; Phenotypes: Tetra-amelia syndrome 1, MIM# 273395; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:42:01.563130+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WNT3 as ready","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:42:01.548191+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wnt3 has been classified as Red List (Low Evidence).","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:41:57.500525+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WNT3 were changed from  to Tetra-amelia syndrome 1, MIM# 273395","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:41:25.961565+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WNT3 were set to ","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:41:01.825876+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WNT3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:40:35.446774+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: WNT3 as Red List (low evidence)","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:40:35.432469+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wnt3 has been classified as Red List (Low Evidence).","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:39:54.667757+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WNT3: Rating: RED; Mode of pathogenicity: None; Publications: 14872406; Phenotypes: Tetra-amelia syndrome 1, MIM# 273395; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WNT3","entity_type":"gene"},{"created":"2020-03-04T10:14:38.529609+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2361","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WFS1 were changed from  to Wolfram syndrome 1, MIM# 222300; Wolfram-like syndrome, autosomal dominant, MIM# 614296","entity_name":"WFS1","entity_type":"gene"},{"created":"2020-03-04T10:14:09.910291+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2360","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WFS1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"WFS1","entity_type":"gene"},{"created":"2020-03-04T10:13:16.865428+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2359","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: WFS1 as Amber List (moderate evidence)","entity_name":"WFS1","entity_type":"gene"},{"created":"2020-03-04T10:13:16.852681+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2359","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wfs1 has been classified as Amber List (Moderate Evidence).","entity_name":"WFS1","entity_type":"gene"},{"created":"2020-03-04T10:12:37.004382+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2358","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: WFS1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Wolfram syndrome 1, MIM# 222300, Wolfram-like syndrome, autosomal dominant, MIM# 614296; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"WFS1","entity_type":"gene"},{"created":"2020-03-04T10:06:59.276505+11:00","panel_name":"Congenital Myasthenia","panel_id":3078,"panel_version":"0.17","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: MYO9A: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 26752647, 27259756; Phenotypes: Myasthenic syndrome, congenital, 24, presynaptic (MIM# 618198); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MYO9A","entity_type":"gene"},{"created":"2020-03-04T09:53:50.503653+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2358","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR81 as ready","entity_name":"WDR81","entity_type":"gene"},{"created":"2020-03-04T09:53:50.490462+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2358","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr81 has been classified as Green List (High Evidence).","entity_name":"WDR81","entity_type":"gene"},{"created":"2020-03-04T09:53:43.915839+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2358","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WDR81 were changed from  to Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2, 610185; Hydrocephalus, congenital, 3, with brain anomalies, 617967","entity_name":"WDR81","entity_type":"gene"},{"created":"2020-03-04T09:53:13.630193+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2357","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR81 were set to ","entity_name":"WDR81","entity_type":"gene"},{"created":"2020-03-04T09:52:25.529820+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2356","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WDR81 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"WDR81","entity_type":"gene"},{"created":"2020-03-04T09:48:14.771081+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2355","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR4 as ready","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-03-04T09:48:14.767022+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2355","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Borderline Green rating: three families but two have the same homozygous variant; some functional data to support gene-disease association.","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-03-04T09:48:14.736770+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2355","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr4 has been classified as Green List (High Evidence).","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-03-04T09:46:58.266036+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SPG11 as ready","entity_name":"SPG11","entity_type":"gene"},{"created":"2020-03-04T09:46:58.253178+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spg11 has been classified as Green List (High Evidence).","entity_name":"SPG11","entity_type":"gene"},{"created":"2020-03-04T09:46:50.194384+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SPG11 as Green List (high evidence)","entity_name":"SPG11","entity_type":"gene"},{"created":"2020-03-04T09:46:50.185302+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spg11 has been classified as Green List (High Evidence).","entity_name":"SPG11","entity_type":"gene"},{"created":"2020-03-04T09:46:19.209633+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SPG11 was added\ngene: SPG11 was added to Regression. Sources: Expert Review\nMode of inheritance for gene: SPG11 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SPG11 were set to 21381113; 22554690; 19224311; 18067136; 27820618\nPhenotypes for gene: SPG11 were set to Spastic paraplegia 11, autosomal recessive, MIM#604360; Charcot-Marie-Tooth disease, axonal, type 2X, MIM#616668; Amyotrophic lateral sclerosis 5, juvenile, MIM#602099\nReview for gene: SPG11 was set to GREEN\ngene: SPG11 was marked as current diagnostic\nAdded comment: Complex neurological phenotypes with onset in first and second decade, characterised by gradual deterioration. \nSources: Expert Review","entity_name":"SPG11","entity_type":"gene"},{"created":"2020-03-04T09:29:43.212866+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2355","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR4 as ready","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-03-04T09:29:43.204140+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2355","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr4 has been classified as Green List (High Evidence).","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-03-04T09:29:33.090576+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2355","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WDR4 were set to PubMed: 26416026, 30079490, 29597095, 28617965","entity_name":"WDR4","entity_type":"gene"},{"created":"2020-03-03T20:56:55.319598+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1609","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RS1 as ready","entity_name":"RS1","entity_type":"gene"},{"created":"2020-03-03T20:56:55.305480+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1609","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rs1 has been classified as Green List (High Evidence).","entity_name":"RS1","entity_type":"gene"},{"created":"2020-03-03T20:56:41.543774+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1609","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RS1 were changed from  to Retinoschisis, MIM#312700","entity_name":"RS1","entity_type":"gene"},{"created":"2020-03-03T20:55:48.160172+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1608","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RS1 were set to ","entity_name":"RS1","entity_type":"gene"},{"created":"2020-03-03T20:55:32.157169+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1607","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RS1 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"RS1","entity_type":"gene"},{"created":"2020-03-03T20:54:37.429586+11:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMC1A as ready","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-03-03T20:54:37.417680+11:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smc1a has been classified as Green List (High Evidence).","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-03-03T20:54:32.812778+11:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMC1A were changed from  to Cornelia de Lange syndrome 2, MIM# 300590","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-03-03T20:54:03.215911+11:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMC1A were set to ","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-03-03T20:53:40.722905+11:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMC1A was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-03-03T20:53:10.833054+11:00","panel_name":"Hypertrichosis syndromes","panel_id":120,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMC1A: Rating: GREEN; Mode of pathogenicity: None; Publications: 17273969, 22106055, 19701948, 26752331, 28166369; Phenotypes: Cornelia de Lange syndrome 2, MIM# 300590; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-03-03T20:51:01.271940+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1606","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMC1A as ready","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-03-03T20:51:01.258425+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1606","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smc1a has been classified as Green List (High Evidence).","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-03-03T20:50:52.542702+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1606","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMC1A were changed from  to Cornelia de Lange syndrome 2, MIM# 300590","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-03-03T20:50:34.276149+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1605","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMC1A were set to ","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-03-03T20:47:46.948135+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1604","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMC1A was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"SMC1A","entity_type":"gene"},{"created":"2020-03-03T20:46:05.012409+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AIRE as ready","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-03-03T20:46:05.002828+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aire has been classified as Green List (High Evidence).","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-03-03T20:45:59.202506+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AIRE were changed from  to Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia, MIM#240300","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-03-03T20:45:30.078592+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AIRE was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-03-03T20:44:57.476277+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: AIRE: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia, MIM#240300; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-03-03T20:43:00.505623+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1603","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LOXHD1 as ready","entity_name":"LOXHD1","entity_type":"gene"},{"created":"2020-03-03T20:43:00.492227+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1603","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: loxhd1 has been classified as Green List (High Evidence).","entity_name":"LOXHD1","entity_type":"gene"},{"created":"2020-03-03T20:42:43.289289+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1603","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AIRE as ready","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-03-03T20:42:43.276408+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1603","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: aire has been classified as Green List (High Evidence).","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-03-03T20:42:31.629223+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1603","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AIRE were changed from  to Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia, MIM#240300","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-03-03T20:41:46.468544+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1602","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of pathogenicity for gene: AIRE was changed from  to Other","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-03-03T20:41:21.506587+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1601","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AIRE was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-03-03T20:40:40.462398+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1600","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AIRE was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"AIRE","entity_type":"gene"},{"created":"2020-03-03T20:39:20.052284+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1599","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LOXHD1 were changed from  to Deafness, autosomal recessive 77, MIM# 613079","entity_name":"LOXHD1","entity_type":"gene"},{"created":"2020-03-03T20:39:17.401070+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.328","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LOXHD1 as ready","entity_name":"LOXHD1","entity_type":"gene"},{"created":"2020-03-03T20:39:17.387759+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.328","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: loxhd1 has been classified as Green List (High Evidence).","entity_name":"LOXHD1","entity_type":"gene"},{"created":"2020-03-03T20:39:00.666014+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1598","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LOXHD1 were set to ","entity_name":"LOXHD1","entity_type":"gene"},{"created":"2020-03-03T20:38:37.848179+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1597","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LOXHD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LOXHD1","entity_type":"gene"},{"created":"2020-03-03T20:37:56.854342+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.328","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LOXHD1 were changed from  to Deafness, autosomal recessive 77, MIM# 613079","entity_name":"LOXHD1","entity_type":"gene"},{"created":"2020-03-03T20:37:32.847429+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1596","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LOXHD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 19732867, 25792669; Phenotypes: Deafness, autosomal recessive 77, MIM# 613079; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LOXHD1","entity_type":"gene"},{"created":"2020-03-03T20:37:06.108042+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.327","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LOXHD1 were set to ","entity_name":"LOXHD1","entity_type":"gene"},{"created":"2020-03-03T20:36:05.586367+11:00","panel_name":"Deafness","panel_id":209,"panel_version":"0.326","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LOXHD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LOXHD1","entity_type":"gene"},{"created":"2020-03-03T20:35:15.108311+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1596","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WFS1 as ready","entity_name":"WFS1","entity_type":"gene"},{"created":"2020-03-03T20:35:15.099384+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1596","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wfs1 has been classified as Green List (High Evidence).","entity_name":"WFS1","entity_type":"gene"},{"created":"2020-03-03T20:35:05.225207+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1596","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WFS1 were changed from  to ?Cataract 41; Deafness, autosomal dominant 6/14/38; Wolfram syndrome, autosomal recessive 1; Wolfram-like syndrome, autosomal dominant; {Diabetes mellitus, noninsulin-dependent, association with}","entity_name":"WFS1","entity_type":"gene"},{"created":"2020-03-03T20:34:30.468600+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1595","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WFS1 were set to ","entity_name":"WFS1","entity_type":"gene"},{"created":"2020-03-03T20:34:15.333719+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1594","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: WFS1 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"WFS1","entity_type":"gene"},{"created":"2020-03-03T20:32:04.539851+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIEZO2 as ready","entity_name":"PIEZO2","entity_type":"gene"},{"created":"2020-03-03T20:32:04.526738+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: piezo2 has been classified as Green List (High Evidence).","entity_name":"PIEZO2","entity_type":"gene"},{"created":"2020-03-03T20:32:00.075541+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PIEZO2 were changed from  to Arthrogryposis, distal, with impaired proprioception and touch (MIM # 617146)","entity_name":"PIEZO2","entity_type":"gene"},{"created":"2020-03-03T20:31:29.576361+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PIEZO2 were set to ","entity_name":"PIEZO2","entity_type":"gene"},{"created":"2020-03-03T20:31:00.811854+11:00","panel_name":"Arthrogryposis","panel_id":47,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PIEZO2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PIEZO2","entity_type":"gene"},{"created":"2020-03-03T12:35:05.434616+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1593","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ING3 as ready","entity_name":"ING3","entity_type":"gene"},{"created":"2020-03-03T12:35:05.425702+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1593","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ing3 has been classified as Red List (Low Evidence).","entity_name":"ING3","entity_type":"gene"},{"created":"2020-03-03T12:34:56.595541+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1593","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ING3 as Red List (low evidence)","entity_name":"ING3","entity_type":"gene"},{"created":"2020-03-03T12:34:56.582355+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1593","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ing3 has been classified as Red List (Low Evidence).","entity_name":"ING3","entity_type":"gene"},{"created":"2020-03-03T12:34:33.714419+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1592","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ING3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"ING3","entity_type":"gene"},{"created":"2020-03-03T12:11:18.083367+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1592","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SYN3 as ready","entity_name":"SYN3","entity_type":"gene"},{"created":"2020-03-03T12:11:18.073717+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1592","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: syn3 has been classified as Red List (Low Evidence).","entity_name":"SYN3","entity_type":"gene"},{"created":"2020-03-03T12:11:07.077170+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1592","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SYN3 as Red List (low evidence)","entity_name":"SYN3","entity_type":"gene"},{"created":"2020-03-03T12:11:07.064211+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1592","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: syn3 has been classified as Red List (Low Evidence).","entity_name":"SYN3","entity_type":"gene"},{"created":"2020-03-03T12:10:45.755613+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1591","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SYN3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SYN3","entity_type":"gene"},{"created":"2020-03-03T12:07:09.046297+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1591","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SIM1 as ready","entity_name":"SIM1","entity_type":"gene"},{"created":"2020-03-03T12:07:09.033155+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1591","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sim1 has been classified as Red List (Low Evidence).","entity_name":"SIM1","entity_type":"gene"},{"created":"2020-03-03T12:06:42.340285+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1591","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SIM1 as Red List (low evidence)","entity_name":"SIM1","entity_type":"gene"},{"created":"2020-03-03T12:06:42.327408+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1591","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sim1 has been classified as Red List (Low Evidence).","entity_name":"SIM1","entity_type":"gene"},{"created":"2020-03-03T12:06:17.729628+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1590","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SIM1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SIM1","entity_type":"gene"},{"created":"2020-03-03T11:58:21.532140+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.1590","user_name":"Kristin Rigbye","item_type":"entity","text":"reviewed gene: RS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 15932525, 23453514, 23847049; Phenotypes: Retinoschisis, 312700; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"RS1","entity_type":"gene"}]}