{"count":220212,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1404","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1402","results":[{"created":"2021-02-18T20:39:29.584666+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAP2K1 as ready","entity_name":"MAP2K1","entity_type":"gene"},{"created":"2021-02-18T20:39:29.576814+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: map2k1 has been classified as Amber List (Moderate Evidence).","entity_name":"MAP2K1","entity_type":"gene"},{"created":"2021-02-18T20:39:26.841248+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAP2K1 were changed from Cardio-facio-cutaneous syndrome to vascular malformations","entity_name":"MAP2K1","entity_type":"gene"},{"created":"2021-02-18T20:38:48.803768+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: TSC2.","entity_name":"TSC2","entity_type":"gene"},{"created":"2021-02-18T20:38:31.016077+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: TSC1.","entity_name":"TSC1","entity_type":"gene"},{"created":"2021-02-18T20:38:10.342411+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: PIK3R2.","entity_name":"PIK3R2","entity_type":"gene"},{"created":"2021-02-18T20:37:49.460492+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: NF2.","entity_name":"NF2","entity_type":"gene"},{"created":"2021-02-18T20:37:33.315829+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: NF1.","entity_name":"NF1","entity_type":"gene"},{"created":"2021-02-18T20:37:08.258280+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: MTOR.","entity_name":"MTOR","entity_type":"gene"},{"created":"2021-02-18T20:36:48.805923+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: MAP3K3.","entity_name":"MAP3K3","entity_type":"gene"},{"created":"2021-02-18T20:36:11.981265+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: GNAQ.","entity_name":"GNAQ","entity_type":"gene"},{"created":"2021-02-18T20:35:35.361042+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"panel","text":"Panel types changed to Victorian Clinical Genetics Services; Rare Disease","entity_name":null,"entity_type":null},{"created":"2021-02-18T20:32:11.232184+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSC2 as ready","entity_name":"TSC2","entity_type":"gene"},{"created":"2021-02-18T20:32:11.222269+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tsc2 has been classified as Green List (High Evidence).","entity_name":"TSC2","entity_type":"gene"},{"created":"2021-02-18T20:32:08.262148+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSC2 were changed from  to Tuberous sclerosis-2, MIM# 613254","entity_name":"TSC2","entity_type":"gene"},{"created":"2021-02-18T20:31:59.358346+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TSC2 as Green List (high evidence)","entity_name":"TSC2","entity_type":"gene"},{"created":"2021-02-18T20:31:59.349357+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tsc2 has been classified as Green List (High Evidence).","entity_name":"TSC2","entity_type":"gene"},{"created":"2021-02-18T20:31:51.201695+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TSC2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Tuberous sclerosis-2, MIM# 613254; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TSC2","entity_type":"gene"},{"created":"2021-02-18T20:31:17.438444+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSC1 as ready","entity_name":"TSC1","entity_type":"gene"},{"created":"2021-02-18T20:31:17.430382+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tsc1 has been classified as Green List (High Evidence).","entity_name":"TSC1","entity_type":"gene"},{"created":"2021-02-18T20:31:07.316453+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSC1 were changed from  to Tuberous sclerosis-1, MIM# 191100","entity_name":"TSC1","entity_type":"gene"},{"created":"2021-02-18T20:30:37.926661+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TSC1 as Green List (high evidence)","entity_name":"TSC1","entity_type":"gene"},{"created":"2021-02-18T20:30:37.915775+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tsc1 has been classified as Green List (High Evidence).","entity_name":"TSC1","entity_type":"gene"},{"created":"2021-02-18T20:30:27.389125+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TSC1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Tuberous sclerosis-1, MIM# 191100; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TSC1","entity_type":"gene"},{"created":"2021-02-18T20:29:44.196331+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIK3R2 as ready","entity_name":"PIK3R2","entity_type":"gene"},{"created":"2021-02-18T20:29:44.186175+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pik3r2 has been classified as Green List (High Evidence).","entity_name":"PIK3R2","entity_type":"gene"},{"created":"2021-02-18T20:29:41.376578+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PIK3R2 were changed from  to Megalencephaly syndromes","entity_name":"PIK3R2","entity_type":"gene"},{"created":"2021-02-18T20:29:30.974930+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.32","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PIK3R2 as Green List (high evidence)","entity_name":"PIK3R2","entity_type":"gene"},{"created":"2021-02-18T20:29:30.963303+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.32","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pik3r2 has been classified as Green List (High Evidence).","entity_name":"PIK3R2","entity_type":"gene"},{"created":"2021-02-18T20:29:21.191360+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PIK3R2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Megalencephaly syndromes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PIK3R2","entity_type":"gene"},{"created":"2021-02-18T20:28:37.517609+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AKT3 as ready","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-02-18T20:28:37.504653+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: akt3 has been classified as Green List (High Evidence).","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-02-18T20:28:35.059718+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AKT3 were changed from  to Megalencephaly syndromes","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-02-18T20:28:28.262675+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: AKT3 were set to PMID: 22729224","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-02-18T20:28:06.064754+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: AKT3: Rating: GREEN; Mode of pathogenicity: None; Publications: 28969385; Phenotypes: Megalencephaly syndromes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-02-18T20:27:18.998744+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: AKT3.","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-02-18T20:27:11.680275+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AKT3 as Green List (high evidence)","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-02-18T20:27:11.669273+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: akt3 has been classified as Green List (High Evidence).","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-02-18T20:25:48.664945+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PTPN11 as ready","entity_name":"PTPN11","entity_type":"gene"},{"created":"2021-02-18T20:25:48.652472+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ptpn11 has been classified as Red List (Low Evidence).","entity_name":"PTPN11","entity_type":"gene"},{"created":"2021-02-18T20:25:40.081382+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PTPN11 as Red List (low evidence)","entity_name":"PTPN11","entity_type":"gene"},{"created":"2021-02-18T20:25:40.072052+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ptpn11 has been classified as Red List (Low Evidence).","entity_name":"PTPN11","entity_type":"gene"},{"created":"2021-02-18T20:25:31.785615+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PTPN11: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"PTPN11","entity_type":"gene"},{"created":"2021-02-18T20:24:05.403087+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PMVK were set to 30942823","entity_name":"PMVK","entity_type":"gene"},{"created":"2021-02-18T20:23:53.056206+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: PMVK: Changed publications: 26202976","entity_name":"PMVK","entity_type":"gene"},{"created":"2021-02-18T20:23:35.818726+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PMVK as ready","entity_name":"PMVK","entity_type":"gene"},{"created":"2021-02-18T20:23:35.810938+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pmvk has been classified as Amber List (Moderate Evidence).","entity_name":"PMVK","entity_type":"gene"},{"created":"2021-02-18T20:23:31.110134+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PMVK were changed from Linear porokeratosis to Linear porokeratosis; Porokeratosis 1, multiple types, MIM# 175800","entity_name":"PMVK","entity_type":"gene"},{"created":"2021-02-18T20:23:12.266284+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PMVK: Rating: AMBER; Mode of pathogenicity: None; Publications: Porokeratosis 1, multiple types, MIM#\t175800; Phenotypes: Porokeratosis 1, multiple types, MIM# 175800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PMVK","entity_type":"gene"},{"created":"2021-02-18T19:18:04.527604+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6399","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MVD as ready","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:18:04.516335+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6399","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mvd has been classified as Green List (High Evidence).","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:17:55.464283+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6399","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MVD as Green List (high evidence)","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:17:55.453668+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6399","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mvd has been classified as Green List (High Evidence).","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:17:38.557658+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6398","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MVD was added\ngene: MVD was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: MVD was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: MVD were set to 30942823; 33491095\nPhenotypes for gene: MVD were set to Porokeratosis 7, multiple types, MIM# 614714\nReview for gene: MVD was set to GREEN\nAdded comment: Porokeratoses are a heterogeneous group of keratinization disorders. For linear porokeratosis and disseminated superficial actinic porokeratosis, a heterozygous pathogenic germline variant in a mevalonate pathway gene and a postzygotic second hit mutation present in affected skin have been shown to be the patho-genetic mechanism for the development of the lesions. At least 5 individuals reported. \nSources: Expert list","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:15:20.942096+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MVD as ready","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:15:20.931359+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mvd has been classified as Green List (High Evidence).","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:15:18.954767+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MVD were changed from Linear porokeratosis to Linear porokeratosis; Porokeratosis 7, multiple types, MIM# 614714","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:15:11.138940+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MVD were set to 30942823","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:15:00.431203+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MVD as Green List (high evidence)","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:15:00.419528+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mvd has been classified as Green List (High Evidence).","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:14:52.392961+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MVD: Rating: GREEN; Mode of pathogenicity: None; Publications: 33491095; Phenotypes: Porokeratosis 7, multiple types, MIM# 614714; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MVD","entity_type":"gene"},{"created":"2021-02-18T19:11:11.845867+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IKBKG as ready","entity_name":"IKBKG","entity_type":"gene"},{"created":"2021-02-18T19:11:11.835030+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ikbkg has been classified as Green List (High Evidence).","entity_name":"IKBKG","entity_type":"gene"},{"created":"2021-02-18T19:11:08.076301+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: IKBKG.","entity_name":"IKBKG","entity_type":"gene"},{"created":"2021-02-18T19:10:59.495761+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IKBKG were changed from Ectodermal dysplasia and immunodeficiency 1, 300291; Ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency, 300301; Incontinentia pigmenti, 308300 to Incontinentia pigmenti, 308300","entity_name":"IKBKG","entity_type":"gene"},{"created":"2021-02-18T19:10:29.910346+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IKBKG were set to ","entity_name":"IKBKG","entity_type":"gene"},{"created":"2021-02-18T19:10:11.393048+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IKBKG as Green List (high evidence)","entity_name":"IKBKG","entity_type":"gene"},{"created":"2021-02-18T19:10:11.382873+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ikbkg has been classified as Green List (High Evidence).","entity_name":"IKBKG","entity_type":"gene"},{"created":"2021-02-18T19:10:02.562511+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IKBKG: Rating: GREEN; Mode of pathogenicity: None; Publications: 32908217, 29077987; Phenotypes: Incontinentia pigment, MIM#i 308300; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"IKBKG","entity_type":"gene"},{"created":"2021-02-18T19:07:47.780659+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: FGFR2.","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-02-18T19:07:41.059139+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGFR2 as ready","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-02-18T19:07:41.047570+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr2 has been classified as Green List (High Evidence).","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-02-18T19:07:35.239343+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FGFR2 were changed from Epdermal naevi to Keratinocytic epidermal naevi","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-02-18T19:07:26.990322+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FGFR2 were set to 9728990","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-02-18T19:07:12.304617+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FGFR2 as Green List (high evidence)","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-02-18T19:07:12.289302+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr2 has been classified as Green List (High Evidence).","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-02-18T19:06:37.725587+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FGFR2: Rating: GREEN; Mode of pathogenicity: None; Publications: 31937562, 30580445; Phenotypes: Keratinocytic epidermal naevi; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR2","entity_type":"gene"},{"created":"2021-02-18T19:04:55.144267+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATP2A2 as ready","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2021-02-18T19:04:55.132952+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp2a2 has been classified as Green List (High Evidence).","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2021-02-18T19:04:36.188489+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ATP2A2 were changed from  to Darier disease, MIM# 124200","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2021-02-18T19:04:10.487267+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ATP2A2 were set to ","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2021-02-18T19:03:59.729433+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ATP2A2 as Green List (high evidence)","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2021-02-18T19:03:59.721943+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp2a2 has been classified as Green List (High Evidence).","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2021-02-18T19:03:52.925531+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: ATP2A2.","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2021-02-18T19:03:43.352866+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ATP2A2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30085326, 26154588, 21720150, 12890216; Phenotypes: Darier disease, MIM# 124200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ATP2A2","entity_type":"gene"},{"created":"2021-02-18T19:00:38.221034+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SPRED1 as ready","entity_name":"SPRED1","entity_type":"gene"},{"created":"2021-02-18T19:00:38.209956+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spred1 has been classified as Green List (High Evidence).","entity_name":"SPRED1","entity_type":"gene"},{"created":"2021-02-18T19:00:34.979212+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SPRED1 were changed from Legius syndrome to Legius syndrome, MIM#\t611431","entity_name":"SPRED1","entity_type":"gene"},{"created":"2021-02-18T19:00:26.550847+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: SPRED1.","entity_name":"SPRED1","entity_type":"gene"},{"created":"2021-02-18T19:00:18.077012+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SPRED1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Legius syndrome, MIM# 611431; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SPRED1","entity_type":"gene"},{"created":"2021-02-18T18:55:25.094154+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMO as ready","entity_name":"SMO","entity_type":"gene"},{"created":"2021-02-18T18:55:25.086138+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smo has been classified as Green List (High Evidence).","entity_name":"SMO","entity_type":"gene"},{"created":"2021-02-18T18:55:22.969887+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMO were changed from Curry-Jones syndrome to Curry-Jones syndrome, MIM#601707","entity_name":"SMO","entity_type":"gene"},{"created":"2021-02-18T18:55:11.565265+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMO: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Curry-Jones syndrome, MIM#601707; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SMO","entity_type":"gene"},{"created":"2021-02-18T18:54:48.092735+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: SMO.","entity_name":"SMO","entity_type":"gene"},{"created":"2021-02-18T18:54:31.699509+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RHOA as ready","entity_name":"RHOA","entity_type":"gene"},{"created":"2021-02-18T18:54:31.685383+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rhoa has been classified as Green List (High Evidence).","entity_name":"RHOA","entity_type":"gene"},{"created":"2021-02-18T18:54:25.824921+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: RHOA.","entity_name":"RHOA","entity_type":"gene"},{"created":"2021-02-18T18:54:03.418104+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RHOA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Blaschko-linear hypopigmentation syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RHOA","entity_type":"gene"},{"created":"2021-02-18T18:53:38.293910+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RASA1 as ready","entity_name":"RASA1","entity_type":"gene"}]}