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{
"count": 220212,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1404",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&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"
}
]
}