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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=832",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=830",
"results": [
{
"created": "2022-05-19T15:29:21.661772+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14590",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: GIGYF2 as Amber List (moderate evidence)",
"entity_name": "GIGYF2",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:29:21.650287+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14590",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: gigyf2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GIGYF2",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:29:01.176851+10:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.183",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: GIGYF2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "GIGYF2",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:28:40.181332+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14589",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: GIGYF2: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 18358451; Phenotypes: {Parkinson disease 11} , OMIM # 607688; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GIGYF2",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:27:40.539708+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14589",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HEY2 as ready",
"entity_name": "HEY2",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:27:40.523974+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14589",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hey2 has been classified as Red List (Low Evidence).",
"entity_name": "HEY2",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:25:37.606405+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14589",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HEY2 were changed from congenital heart defects and thoracic aortic aneurysms to congenital heart disease MONDO:0005453; thoracic aortic aneurysms",
"entity_name": "HEY2",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:24:09.444992+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14588",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: GCH1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 7874165, 11113234, 15753436, 9667588, 10987649, 32170445, 32278297, 32746945, 30314816; Phenotypes: Hyperphenylalaninemia, BH4-deficient, B, MIM# 233910, Dystonia, DOPA-responsive, with or without hyperphenylalaninemia, MIM# 128230; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "GCH1",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:23:54.964598+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IL18BP as ready",
"entity_name": "IL18BP",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:23:54.951742+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: il18bp has been classified as Red List (Low Evidence).",
"entity_name": "IL18BP",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:23:07.470485+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ITPKB as ready",
"entity_name": "ITPKB",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:23:07.458941+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: itpkb has been classified as Red List (Low Evidence).",
"entity_name": "ITPKB",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:22:58.068757+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ITPKB were changed from Severe combined immunodeficiency, absent T cells, present B cells and NK cells to Severe combined immunodeficiency MONDO:0015974, absent T cells, present B cells and NK cells",
"entity_name": "ITPKB",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:20:58.778753+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14587",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MUC7 as ready",
"entity_name": "MUC7",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:20:58.764898+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14587",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: muc7 has been classified as Red List (Low Evidence).",
"entity_name": "MUC7",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:20:47.983485+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14587",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MUC7 were changed from to {Asthma, protection against} MIM#600807",
"entity_name": "MUC7",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:20:24.792026+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14586",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MUC7 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MUC7",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:19:25.192210+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14585",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYF6 as ready",
"entity_name": "MYF6",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:19:25.179503+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14585",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myf6 has been classified as Red List (Low Evidence).",
"entity_name": "MYF6",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:19:15.899330+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14585",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYF6 were changed from to Centronuclear myopathy, MONDO:0018947",
"entity_name": "MYF6",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:18:21.954919+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14584",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYF6 were set to ",
"entity_name": "MYF6",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:17:59.867601+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14583",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYF6 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYF6",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:16:31.310179+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14582",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDCD6IP as ready",
"entity_name": "PDCD6IP",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:16:31.296941+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14582",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pdcd6ip has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDCD6IP",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:16:21.887441+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14582",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDCD6IP were changed from Microcephaly; intellectual disability to Neurodevelopmental disorder MONDO:0700092; Microcephaly; intellectual disability",
"entity_name": "PDCD6IP",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:15:24.708158+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14581",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDCD6IP as Amber List (moderate evidence)",
"entity_name": "PDCD6IP",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:15:24.696751+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14581",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pdcd6ip has been classified as Amber List (Moderate Evidence).",
"entity_name": "PDCD6IP",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:14:15.816327+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14580",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POU5F1 as ready",
"entity_name": "POU5F1",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:14:15.804008+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14580",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pou5f1 has been classified as Red List (Low Evidence).",
"entity_name": "POU5F1",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:14:14.620139+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14580",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: GBA2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 23332916, 23332917, 29524657; Phenotypes: Spastic paraplegia 46, autosomal recessive, MIM# 614409, MONDO:0013737; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GBA2",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:13:37.851724+10:00",
"panel_name": "Ataxia - paediatric",
"panel_id": 271,
"panel_version": "0.337",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: GBA2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 23332916, 23332917, 29524657; Phenotypes: Spastic paraplegia 46, autosomal recessive, MIM# 614409, MONDO:0013737; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GBA2",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:11:25.601702+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14580",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Classified gene: GATAD1 as Red List (low evidence)",
"entity_name": "GATAD1",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:11:25.588931+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14580",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "Gene: gatad1 has been classified as Red List (Low Evidence).",
"entity_name": "GATAD1",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:11:02.992733+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SGK3 as ready",
"entity_name": "SGK3",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:11:02.957511+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sgk3 has been classified as Red List (Low Evidence).",
"entity_name": "SGK3",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:11:02.655026+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: GATAD1: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 21965549; Phenotypes: ?Cardiomyopathy, dilated, 2B, OMIM # 614672; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GATAD1",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:09:39.431248+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DMPK as ready",
"entity_name": "DMPK",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:09:39.415141+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dmpk has been removed from the panel.",
"entity_name": "DMPK",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:09:07.408866+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NOP56 as ready",
"entity_name": "NOP56",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:09:07.395341+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nop56 has been removed from the panel.",
"entity_name": "NOP56",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:08:56.166522+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag STR tag was added to gene: NOP56.",
"entity_name": "NOP56",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:08:29.892844+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: GAN: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 11062483; Phenotypes: Giant axonal neuropathy-1, MIM# 256850; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GAN",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:08:16.722592+10:00",
"panel_name": "Hereditary Neuropathy - complex",
"panel_id": 3070,
"panel_version": "0.125",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: GAN: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 11062483; Phenotypes: Giant axonal neuropathy-1, MIM# 256850; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GAN",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:06:48.745575+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Chirag Patel",
"item_type": "entity",
"text": "reviewed gene: GALNT3: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 15133511, 20358599, 32125652; Phenotypes: Tumoral calcinosis, hyperphosphatemic, familial, 1, MIM# 211900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GALNT3",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:00:55.387694+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPD1 as ready",
"entity_name": "GPD1",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:00:55.374796+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpd1 has been classified as Green List (High Evidence).",
"entity_name": "GPD1",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:00:41.990645+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14579",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GPD1 were changed from to Hypertriglyceridemia, transient infantile MIM#614480; glycerol-3-phosphate dehydrogenase deficiency",
"entity_name": "GPD1",
"entity_type": "gene"
},
{
"created": "2022-05-19T15:00:19.064920+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14578",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GPD1 were set to ",
"entity_name": "GPD1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:59:15.386385+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14577",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GPD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GPD1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:58:52.339740+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14576",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GPD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 22226083, 24549054, 35365473, 34484308, 33447932; Phenotypes: Hypertriglyceridaemia, transient infantile, MIM# 614480; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GPD1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:56:15.174442+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14576",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPHN as ready",
"entity_name": "GPHN",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:56:15.160320+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14576",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gphn has been classified as Green List (High Evidence).",
"entity_name": "GPHN",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:55:55.004237+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14576",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GPHN were set to 22040219; 11095995; 26613940; 24561070; 23393157",
"entity_name": "GPHN",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:54:43.515982+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14575",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GPNMB as ready",
"entity_name": "GPNMB",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:54:43.504134+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14575",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gpnmb has been classified as Green List (High Evidence).",
"entity_name": "GPNMB",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:54:33.825069+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14575",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GPNMB were changed from to Amyloidosis, primary localized cutaneous, 3, MIM# 617920",
"entity_name": "GPNMB",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:54:12.804632+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GPNMB were set to ",
"entity_name": "GPNMB",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:53:52.856807+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14573",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GPNMB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GPNMB",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:53:29.188876+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14572",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GPNMB: Rating: GREEN; Mode of pathogenicity: None; Publications: 29336782; Phenotypes: Amyloidosis, primary localized cutaneous, 3, MIM# 617920; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GPNMB",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:51:39.287932+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14572",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GREM1 as ready",
"entity_name": "GREM1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:51:39.275364+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14572",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: grem1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GREM1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:51:25.661969+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14572",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GREM1 were changed from to Genetic intestinal polyposis MONDO:0018188",
"entity_name": "GREM1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:50:30.689297+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14571",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GREM1 were set to ",
"entity_name": "GREM1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:50:08.120618+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14570",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GREM1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GREM1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:49:48.585423+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14569",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag SV/CNV tag was added to gene: GREM1.",
"entity_name": "GREM1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:49:33.416363+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14569",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GREM1 as Amber List (moderate evidence)",
"entity_name": "GREM1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:49:33.398736+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14569",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: grem1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GREM1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:29:36.049551+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14568",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRAP as ready",
"entity_name": "MRAP",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:29:36.037236+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14568",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrap has been classified as Green List (High Evidence).",
"entity_name": "MRAP",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:29:27.900868+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14568",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MRAP were changed from to Glucocorticoid deficiency 2, MIM# 607398",
"entity_name": "MRAP",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:29:05.168414+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14567",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MRAP were set to ",
"entity_name": "MRAP",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:28:43.317642+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14566",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MRAP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MRAP",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:28:20.803579+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14565",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MRAP: Rating: GREEN; Mode of pathogenicity: None; Publications: 15654338; Phenotypes: Glucocorticoid deficiency 2, MIM# 607398; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MRAP",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:25:50.263312+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14565",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPZL2 as ready",
"entity_name": "MPZL2",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:25:50.237613+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14565",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpzl2 has been classified as Green List (High Evidence).",
"entity_name": "MPZL2",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:23:52.902110+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14565",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MPZL2 were changed from to Deafness, autosomal recessive 111, MIM#618145",
"entity_name": "MPZL2",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:23:24.185082+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14564",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MPZL2 were set to ",
"entity_name": "MPZL2",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:22:59.945002+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14563",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MPZL2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MPZL2",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:22:35.074877+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14562",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MPZL2: Rating: GREEN; Mode of pathogenicity: None; Publications: 29982980, 29961571; Phenotypes: Deafness, autosomal recessive 111, MIM#618145; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MPZL2",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:21:37.051616+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPC1 as ready",
"entity_name": "MPC1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:21:37.018950+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpc1 has been classified as Green List (High Evidence).",
"entity_name": "MPC1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:21:32.645997+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.821",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MPC1 were changed from Mitochondrial pyruvate carrier deficiency, MIM# 614741 to Mitochondrial pyruvate carrier deficiency, MIM# 614741",
"entity_name": "MPC1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:17:02.525699+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14562",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPZ as ready",
"entity_name": "MPZ",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:17:02.513014+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14562",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpz has been classified as Green List (High Evidence).",
"entity_name": "MPZ",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:16:51.263031+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14562",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MPZ were changed from to Charcot Marie Tooth disease, dominant intermediate D, 60779; Neuropathy, congenital hypomyelinating, 605253; Charcot Marie Tooth disease, type 2J, 607736; Dejerine Sottas disease, 145900; Charcot Marie Tooth disease, type 1B, 118200; Charcot Marie Tooth disease, type 2I, 607677; HMSN",
"entity_name": "MPZ",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:16:07.232056+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14561",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MPZ were set to ",
"entity_name": "MPZ",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:15:41.846416+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14560",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MPZ was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MPZ",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:15:20.320947+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.820",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MPC1 were changed from Mitochondrial pyruvate carrier deficiency, MIM# 614741 to Mitochondrial pyruvate carrier deficiency, MIM# 614741",
"entity_name": "MPC1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:14:04.530041+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.819",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MPC1 were changed from to Mitochondrial pyruvate carrier deficiency, MIM# 614741",
"entity_name": "MPC1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:13:05.553763+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.818",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MPC1 were set to ",
"entity_name": "MPC1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:12:16.900953+10:00",
"panel_name": "Mitochondrial disease",
"panel_id": 203,
"panel_version": "0.817",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MPC1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MPC1",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:10:03.299506+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPV17 as ready",
"entity_name": "MPV17",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:10:03.283326+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpv17 has been classified as Green List (High Evidence).",
"entity_name": "MPV17",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:09:50.493432+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14559",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MPV17 were changed from to Charcot-Marie-Tooth disease, axonal, type 2EE, MIM# 618400",
"entity_name": "MPV17",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:09:20.827881+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14558",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MPV17 were set to ",
"entity_name": "MPV17",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:08:46.616593+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14557",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MPV17 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MPV17",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:03:27.320362+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14556",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MPO as ready",
"entity_name": "MPO",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:03:27.299181+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14556",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mpo has been classified as Amber List (Moderate Evidence).",
"entity_name": "MPO",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:03:13.653686+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14556",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MPO were changed from to Myeloperoxidase deficiency, MIM# 254600",
"entity_name": "MPO",
"entity_type": "gene"
},
{
"created": "2022-05-19T14:02:42.069331+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14555",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MPO was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MPO",
"entity_type": "gene"
}
]
}