{"count":220212,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1405","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1403","results":[{"created":"2021-02-18T18:53:38.285766+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rasa1 has been classified as Amber List (Moderate Evidence).","entity_name":"RASA1","entity_type":"gene"},{"created":"2021-02-18T18:53:23.002989+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RASA1 as Amber List (moderate evidence)","entity_name":"RASA1","entity_type":"gene"},{"created":"2021-02-18T18:53:22.995646+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rasa1 has been classified as Amber List (Moderate Evidence).","entity_name":"RASA1","entity_type":"gene"},{"created":"2021-02-18T18:53:14.357403+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RASA1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Capillary malformation-arteriovenous malformation syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RASA1","entity_type":"gene"},{"created":"2021-02-18T18:52:42.540890+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: PTEN.","entity_name":"PTEN","entity_type":"gene"},{"created":"2021-02-18T18:52:26.814438+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PTEN as ready","entity_name":"PTEN","entity_type":"gene"},{"created":"2021-02-18T18:52:26.806924+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pten has been classified as Green List (High Evidence).","entity_name":"PTEN","entity_type":"gene"},{"created":"2021-02-18T18:52:17.149309+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PTEN: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Epidermal naevi, Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, Melanoma; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PTEN","entity_type":"gene"},{"created":"2021-02-18T18:51:42.759657+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIK3CA as ready","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2021-02-18T18:51:42.751473+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pik3ca has been classified as Green List (High Evidence).","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2021-02-18T18:51:39.422078+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PIK3CA were changed from Vascular malformations; PIK3CA-related overgrowth syndromes to Vascular malformations; PIK3CA-related overgrowth syndromes; CLAPO syndrome, somatic 613089; CLOVE syndrome, somatic 612918; Nevus, epidermal, somatic 162900","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2021-02-18T18:51:27.984686+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: PIK3CA.","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2021-02-18T18:51:19.574924+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PIK3CA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Vascular malformations, PIK3CA-related overgrowth syndromes, CLAPO syndrome, somatic 613089, CLOVE syndrome, somatic 612918, Nevus, epidermal, somatic 162900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2021-02-18T18:49:58.554668+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: NRAS.","entity_name":"NRAS","entity_type":"gene"},{"created":"2021-02-18T18:49:52.003174+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NRAS as ready","entity_name":"NRAS","entity_type":"gene"},{"created":"2021-02-18T18:49:51.995086+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nras has been classified as Green List (High Evidence).","entity_name":"NRAS","entity_type":"gene"},{"created":"2021-02-18T18:49:37.626192+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NRAS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Melanocytic naevi, Congenital melanocytic naevus syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NRAS","entity_type":"gene"},{"created":"2021-02-18T18:49:11.181643+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NF2 as ready","entity_name":"NF2","entity_type":"gene"},{"created":"2021-02-18T18:49:11.166687+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nf2 has been classified as Green List (High Evidence).","entity_name":"NF2","entity_type":"gene"},{"created":"2021-02-18T18:49:05.316871+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NF2 were changed from NF2; NEUROFIBROMATOSIS, TYPE II to Schwannomatosis, somatic 162091; Meningioma, NF2-related, somatic 607174; Neurofibromatosis, type 2 101000","entity_name":"NF2","entity_type":"gene"},{"created":"2021-02-18T18:48:45.200318+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NF2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NF2","entity_type":"gene"},{"created":"2021-02-18T18:48:35.497582+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: NF2: Changed publications: 29409008","entity_name":"NF2","entity_type":"gene"},{"created":"2021-02-18T18:48:21.155972+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NF2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Schwannomatosis, somatic 162091, Meningioma, NF2-related, somatic 607174, Neurofibromatosis, type 2 101000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NF2","entity_type":"gene"},{"created":"2021-02-18T18:46:52.534877+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NF1 as ready","entity_name":"NF1","entity_type":"gene"},{"created":"2021-02-18T18:46:52.527162+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nf1 has been classified as Green List (High Evidence).","entity_name":"NF1","entity_type":"gene"},{"created":"2021-02-18T18:46:50.412831+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NF1 were changed from Neurofibromatosis type I to Neurofibromatosis type I, MIM#162200","entity_name":"NF1","entity_type":"gene"},{"created":"2021-02-18T18:46:40.260972+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: NF1: Changed phenotypes: Neurofibromatosis type I, MIM#162200","entity_name":"NF1","entity_type":"gene"},{"created":"2021-02-18T18:45:50.215124+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NF1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurofibromatosis type I; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NF1","entity_type":"gene"},{"created":"2021-02-18T18:45:00.650303+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTOR as ready","entity_name":"MTOR","entity_type":"gene"},{"created":"2021-02-18T18:45:00.637953+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mtor has been classified as Green List (High Evidence).","entity_name":"MTOR","entity_type":"gene"},{"created":"2021-02-18T18:44:52.783195+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MTOR: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypomelanosis of Ito/Blaschko-linear hypopigmentation; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MTOR","entity_type":"gene"},{"created":"2021-02-18T18:44:15.451000+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAP3K3 as ready","entity_name":"MAP3K3","entity_type":"gene"},{"created":"2021-02-18T18:44:15.439831+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: map3k3 has been classified as Green List (High Evidence).","entity_name":"MAP3K3","entity_type":"gene"},{"created":"2021-02-18T18:44:04.021566+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MAP3K3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Verrucous haemangiomas; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MAP3K3","entity_type":"gene"},{"created":"2021-02-18T18:43:37.297334+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: GNAS.","entity_name":"GNAS","entity_type":"gene"},{"created":"2021-02-18T18:43:03.469782+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"panel","text":"Panel types changed to Rare Disease","entity_name":null,"entity_type":null},{"created":"2021-02-18T18:41:33.724422+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MAP2K1 as Amber List (moderate evidence)","entity_name":"MAP2K1","entity_type":"gene"},{"created":"2021-02-18T18:41:33.714660+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.5","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":"2021-02-18T18:41:11.785837+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MAP2K1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: vascular malformations; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MAP2K1","entity_type":"gene"},{"created":"2021-02-18T18:39:58.535424+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT10 as ready","entity_name":"KRT10","entity_type":"gene"},{"created":"2021-02-18T18:39:58.524742+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt10 has been classified as Green List (High Evidence).","entity_name":"KRT10","entity_type":"gene"},{"created":"2021-02-18T18:39:49.940860+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: KRT10: Changed phenotypes: Epidermolytic hyperkeratosis MIM#113800, Pachyonychia congenita, Ichythosis with confetti, MIM#609165, Palmoplantar keratoderma","entity_name":"KRT10","entity_type":"gene"},{"created":"2021-02-18T18:38:52.632125+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT10: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Epidermolytic hyperkeratosis, Pachyonychia congenita, Ichythosis with confetti, Palmoplantar keratoderma; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT10","entity_type":"gene"},{"created":"2021-02-18T18:38:30.288274+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT1 as ready","entity_name":"KRT1","entity_type":"gene"},{"created":"2021-02-18T18:38:30.269330+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt1 has been classified as Green List (High Evidence).","entity_name":"KRT1","entity_type":"gene"},{"created":"2021-02-18T18:38:26.119236+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: KRT1.","entity_name":"KRT1","entity_type":"gene"},{"created":"2021-02-18T18:38:15.569498+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Ichthyosis histrix, Epidermolytic hyperkeratosis, Palmoplantar keratoderma; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT1","entity_type":"gene"},{"created":"2021-02-18T18:37:54.481276+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRAS as ready","entity_name":"KRAS","entity_type":"gene"},{"created":"2021-02-18T18:37:54.470313+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kras has been classified as Green List (High Evidence).","entity_name":"KRAS","entity_type":"gene"},{"created":"2021-02-18T18:37:49.698357+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: KRAS.","entity_name":"KRAS","entity_type":"gene"},{"created":"2021-02-18T18:37:38.651635+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRAS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Epidermal naevi, Schimmelpenning syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRAS","entity_type":"gene"},{"created":"2021-02-18T18:37:05.327363+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IDH2 as ready","entity_name":"IDH2","entity_type":"gene"},{"created":"2021-02-18T18:37:05.319109+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: idh2 has been classified as Green List (High Evidence).","entity_name":"IDH2","entity_type":"gene"},{"created":"2021-02-18T18:37:00.461254+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: IDH2.","entity_name":"IDH2","entity_type":"gene"},{"created":"2021-02-18T18:36:53.217076+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IDH2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Maffucci syndrome, Ollier disease; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"IDH2","entity_type":"gene"},{"created":"2021-02-18T18:36:32.582137+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IDH1 as ready","entity_name":"IDH1","entity_type":"gene"},{"created":"2021-02-18T18:36:32.568683+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: idh1 has been classified as Green List (High Evidence).","entity_name":"IDH1","entity_type":"gene"},{"created":"2021-02-18T18:36:27.424120+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: IDH1.","entity_name":"IDH1","entity_type":"gene"},{"created":"2021-02-18T18:36:19.249460+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IDH1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Maffucci syndrome, Ollier disease; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"IDH1","entity_type":"gene"},{"created":"2021-02-18T18:35:51.882400+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HRAS as ready","entity_name":"HRAS","entity_type":"gene"},{"created":"2021-02-18T18:35:51.872238+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hras has been classified as Green List (High Evidence).","entity_name":"HRAS","entity_type":"gene"},{"created":"2021-02-18T18:35:47.618205+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: HRAS.","entity_name":"HRAS","entity_type":"gene"},{"created":"2021-02-18T18:35:38.639115+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HRAS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Phakomatosis pigmentokeratotica, Epidermal naevi, Woolly hair, Costello syndrome, Schimmelpenning syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HRAS","entity_type":"gene"},{"created":"2021-02-18T18:35:02.960830+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GNAS as ready","entity_name":"GNAS","entity_type":"gene"},{"created":"2021-02-18T18:35:02.950595+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gnas has been classified as Green List (High Evidence).","entity_name":"GNAS","entity_type":"gene"},{"created":"2021-02-18T18:34:59.679906+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GNAS were set to 12970318","entity_name":"GNAS","entity_type":"gene"},{"created":"2021-02-18T18:34:34.938840+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GNAS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: McCune-Albright syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GNAS","entity_type":"gene"},{"created":"2021-02-18T18:34:09.957231+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GNAQ as ready","entity_name":"GNAQ","entity_type":"gene"},{"created":"2021-02-18T18:34:09.947651+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gnaq has been classified as Green List (High Evidence).","entity_name":"GNAQ","entity_type":"gene"},{"created":"2021-02-18T18:34:01.566339+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GNAQ: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Extensive dermal melanocytosis, Sturge Weber syndrome, Phakomatosis pigmentovascularis; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GNAQ","entity_type":"gene"},{"created":"2021-02-18T18:33:36.178710+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GNA14 as ready","entity_name":"GNA14","entity_type":"gene"},{"created":"2021-02-18T18:33:36.159022+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gna14 has been classified as Green List (High Evidence).","entity_name":"GNA14","entity_type":"gene"},{"created":"2021-02-18T18:33:32.276446+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: GNA14.","entity_name":"GNA14","entity_type":"gene"},{"created":"2021-02-18T18:33:20.840041+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GNA14: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Kaposiform endothelioma, Tufted angioma; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GNA14","entity_type":"gene"},{"created":"2021-02-18T18:32:43.394122+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GNA11 as ready","entity_name":"GNA11","entity_type":"gene"},{"created":"2021-02-18T18:32:43.380937+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gna11 has been classified as Green List (High Evidence).","entity_name":"GNA11","entity_type":"gene"},{"created":"2021-02-18T18:32:38.837762+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: GNA11.","entity_name":"GNA11","entity_type":"gene"},{"created":"2021-02-18T18:32:29.443817+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GNA11: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Extensive dermal melanocytosis, Phakomatosis pigmentovascularis; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GNA11","entity_type":"gene"},{"created":"2021-02-18T18:32:04.982780+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: ACTB.","entity_name":"ACTB","entity_type":"gene"},{"created":"2021-02-18T18:31:43.935452+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: AKT1.","entity_name":"AKT1","entity_type":"gene"},{"created":"2021-02-18T18:31:35.527086+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: FGFR1.","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-02-18T18:31:25.506433+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGFR3 as ready","entity_name":"FGFR3","entity_type":"gene"},{"created":"2021-02-18T18:31:25.498993+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr3 has been classified as Green List (High Evidence).","entity_name":"FGFR3","entity_type":"gene"},{"created":"2021-02-18T18:31:18.863628+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: FGFR3.","entity_name":"FGFR3","entity_type":"gene"},{"created":"2021-02-18T18:31:10.555432+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FGFR3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Epidermal naevi, Syringocystadenoma papilliferum; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR3","entity_type":"gene"},{"created":"2021-02-18T18:30:36.434680+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FGFR1 as ready","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-02-18T18:30:36.420823+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fgfr1 has been classified as Green List (High Evidence).","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-02-18T18:30:29.121851+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FGFR1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Epidermal naevi; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR1","entity_type":"gene"},{"created":"2021-02-18T18:29:54.587198+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AKT1 as ready","entity_name":"AKT1","entity_type":"gene"},{"created":"2021-02-18T18:29:54.572336+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: akt1 has been classified as Green List (High Evidence).","entity_name":"AKT1","entity_type":"gene"},{"created":"2021-02-18T18:29:52.430672+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AKT1 were changed from Proteus syndrome to Proteus syndrome, somatic\t176920","entity_name":"AKT1","entity_type":"gene"},{"created":"2021-02-18T18:29:39.387529+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: AKT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 33030203; Phenotypes: Proteus syndrome, somatic 176920; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"AKT1","entity_type":"gene"},{"created":"2021-02-18T18:28:53.350166+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACTB as ready","entity_name":"ACTB","entity_type":"gene"},{"created":"2021-02-18T18:28:53.341535+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: actb has been classified as Green List (High Evidence).","entity_name":"ACTB","entity_type":"gene"},{"created":"2021-02-18T18:28:51.660910+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ACTB were changed from  to Becker's naevus","entity_name":"ACTB","entity_type":"gene"},{"created":"2021-02-18T17:33:35.463315+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.1","user_name":"Mathew Wallis","item_type":"entity","text":"edited their review of gene: PIK3R2: Changed publications: PMID: 22729224","entity_name":"PIK3R2","entity_type":"gene"},{"created":"2021-02-18T17:33:22.600609+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.1","user_name":"Mathew Wallis","item_type":"entity","text":"edited their review of gene: PIK3R2: Changed publications: PMID: 22729224, PMID: 22729224","entity_name":"PIK3R2","entity_type":"gene"},{"created":"2021-02-18T17:33:04.783337+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.1","user_name":"Mathew Wallis","item_type":"entity","text":"gene: AKT3 was added\ngene: AKT3 was added to Mosaic skin disorders. Sources: Literature\nMode of inheritance for gene: AKT3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: AKT3 were set to PMID: 22729224\nReview for gene: AKT3 was set to GREEN\nAdded comment: Sources: Literature","entity_name":"AKT3","entity_type":"gene"},{"created":"2021-02-18T17:29:36.397841+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.1","user_name":"Mathew Wallis","item_type":"entity","text":"changed review comment from: Sources: Literature, Expert Review; to: Sources: Literature","entity_name":"TSC2","entity_type":"gene"},{"created":"2021-02-18T17:29:24.736081+11:00","panel_name":"Mosaic skin disorders","panel_id":3472,"panel_version":"0.1","user_name":"Mathew Wallis","item_type":"entity","text":"changed review comment from: Sources: Expert Review, Literature; to: Sources: Literature","entity_name":"TSC1","entity_type":"gene"}]}